Cerebral Palsy

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Template:Short description Template:Use dmy dates Template:Infobox medical condition (new) Cerebral palsy (CP) is a group of movement disorders that appear in early childhood.<ref name="NINDS2013" /> Signs and symptoms vary among people and over time,<ref name="NINDS2013" /><ref>Template:Cite journal</ref> but include poor coordination, stiff muscles, weak muscles, and tremors.<ref name="NINDS2013" /> There may be problems with sensation, vision, hearing, and speaking.<ref name="NINDS2013" /> Often, babies with cerebral palsy do not roll over, sit, crawl or walk as early as other children of their age.<ref name="NINDS2013" /> Other symptoms include seizures and problems with thinking or reasoning, which each occur in about one-third of people with CP.<ref name="NINDS2013" /> While symptoms may get more noticeable over the first few years of life, underlying problems do not worsen over time.<ref name="NINDS2013" />

Cerebral palsy is caused by abnormal development or damage to the parts of the brain that control movement, balance, and posture.<ref name="NINDS2013" /><ref>Template:Cite web</ref> Most often, the problems occur during pregnancy, but they may also occur during childbirth or shortly after birth.<ref name="NINDS2013" /> Often, the cause is unknown.<ref name="NINDS2013" /> Risk factors include preterm birth, being a twin, certain infections during pregnancy, such as toxoplasmosis or rubella, exposure to methylmercury during pregnancy, a difficult delivery, and head trauma during the first few years of life, among others.<ref name="NINDS2013" /> About 2% of cases are believed to be due to an inherited genetic cause.<ref name="omim" /> A number of sub-types are classified, based on the specific problems present.<ref name="NINDS2013" /> For example, those with stiff muscles have spastic cerebral palsy, those with poor coordination in locomotion have ataxic cerebral palsy, and those with writhing movements have dyskinetic cerebral palsy.<ref>Template:Cite journal</ref> Diagnosis is based on the child's development over time.<ref name="NINDS2013" /> Blood tests and medical imaging may be used to rule out other possible causes.<ref name="NINDS2013" />

CP is partly preventable through immunization of the mother, and efforts to prevent head injuries in children such as through improved safety.<ref name="NINDS2013" /> There is no known cure for CP, but supportive treatments, medication and surgery may help many individuals.<ref name="NINDS2013" /> This may include physical therapy, occupational therapy and speech therapy.<ref name="NINDS2013" /> Medications such as diazepam, baclofen and botulinum toxin may help relax stiff muscles.<ref name="NINDS2013" /><ref name=Farag2020>Template:Cite journal</ref><ref>Template:Cite journal</ref> Surgery may include lengthening muscles and cutting overly active nerves.<ref name="NINDS2013" /> Often, external braces and other assistive technology are helpful.<ref name="NINDS2013" /> Some affected children can achieve near normal adult lives with appropriate treatment.<ref name="NINDS2013" /> While alternative medicines are frequently used, there is no evidence to support their use.<ref name="NINDS2013" />

Cerebral palsy is the most common movement disorder in children.<ref>Template:Cite web</ref> It occurs in about 2.1 per 1,000 live births.<ref name="Osk2013" /> Cerebral palsy has been documented throughout history, with the first known descriptions occurring in the work of Hippocrates in the 5th century BCE.<ref name="History2013" /> Extensive study of the condition began in the 19th century by William John Little, after whom spastic diplegia was called "Little's disease".<ref name="History2013" /> William Osler first named it "cerebral palsy" from the German Template:Lang (cerebral child-paralysis).<ref>Template:Cite web</ref> A number of potential treatments are being examined, including stem cell therapy.<ref name="NINDS2013" /> However, more research is required to determine if it is effective and safe.<ref name="NINDS2013" /> Template:TOC limit

Signs and symptoms[edit | edit source]

Cerebral palsy is defined as "a group of permanent disorders of the development of movement and posture, causing activity limitation, that are attributed to non-progressive disturbances that occurred in the developing fetal or infant brain."<ref name="pmid17370477" /> While movement problems are the central feature of CP, difficulties with thinking, learning, feeling, communication and behavior often co-occur,<ref name="pmid17370477" /> with 28% having epilepsy, 58% having difficulties with communication, at least 42% having problems with their vision, and 23Template:Endash56% having learning disabilities.<ref name="kent_2013" /> Muscle contractions in people with cerebral palsy are commonly thought to arise from overactivation.<ref>Template:Cite journal</ref>

Cerebral palsy is characterized by abnormal muscle tone, reflexes, or motor development and coordination. The neurological lesion is primary and permanent while orthopedic manifestations are secondary and progressive. In cerebral palsy unequal growth between muscle-tendon units and bone eventually leads to bone and joint deformities. At first, deformities are dynamic. Over time, deformities tend to become static, and joint contractures develop. Deformities in general and static deformities in specific (joint contractures) cause increasing gait difficulties in the form of tip-toeing gait, due to tightness of the Achilles tendon, and scissoring gait, due to tightness of the hip adductors. These gait patterns are among the most common gait abnormalities in children with cerebral palsy. However, orthopaedic manifestations of cerebral palsy are diverse.<ref name="elsobky2017" /><ref name="argawal&verma2012" /> Additionally, crouch gait (excessive knee flexion gait) is prevalent among children who possess the ability to walk.<ref name="Amen2018" /> The effects of cerebral palsy fall on a continuum of motor dysfunction, which may range from slight clumsiness at the mild end of the spectrum to impairments so severe that they render coordinated movement virtually impossible at the other end of the spectrum.<ref>Template:Cite book</ref> Although most people with CP have problems with increased muscle tone, some have normal or low muscle tone. High muscle tone can either be due to spasticity or dystonia.<ref>Template:Cite journal</ref>

Babies born with severe cerebral palsy often have irregular posture; their bodies may be either very floppy or very stiff. Birth defects, such as spinal curvature, a small jawbone, or a small head sometimes occur along with CP. Symptoms may appear or change as a child gets older. Babies born with cerebral palsy do not immediately present with symptoms.<ref>Template:Cite web</ref> Classically, CP becomes evident when the baby reaches the developmental stage at 6 to 9 months and is starting to mobilise, where preferential use of limbs, asymmetry, or gross motor developmental delay is seen.<ref name="argawal&verma2012" />

Drooling is common among children with cerebral palsy, which can have a variety of impacts including social rejection, impaired speaking, damage to clothing and books, and mouth infections.<ref>Template:Cite journal</ref> It can additionally cause choking.<ref name="auto" />

An average of 55.5% of people with cerebral palsy experience lower urinary tract symptoms, more commonly excessive storage issues than voiding issues. Those with voiding issues and pelvic floor overactivity can deteriorate as adults and experience upper urinary tract dysfunction.<ref>Template:Cite journal</ref>

Children with CP may also have sensory processing issues.<ref>Template:Cite book</ref> Adults with cerebral palsy have a higher risk of respiratory failure.<ref>Template:Cite book</ref>

Skeleton[edit | edit source]

For bones to attain their normal shape and size, they require the stresses from normal musculature.<ref name="Mughal2014" /> People with cerebral palsy are at risk of low bone mineral density.<ref>Template:Cite journal</ref> The shafts of the bones are often thin (gracile),<ref name="Mughal2014" /> and become thinner during growth. When compared to these thin shafts (diaphyses), the centres (metaphyses) often appear quite enlarged (ballooning).Template:Citation needed Due to more than normal joint compression caused by muscular imbalances, articular cartilage may atrophy,<ref name="Kerkovich, D 2009, pp. 41-53" />Template:Rp leading to narrowed joint spaces. Depending on the degree of spasticity, a person with CP may exhibit a variety of angular joint deformities. Because vertebral bodies need vertical gravitational loading forces to develop properly, spasticity and an abnormal gait can hinder proper or full bone and skeletal development. People with CP tend to be shorter in height than the average person because their bones are not allowed to grow to their full potential. Sometimes bones grow to different lengths, so the person may have one leg longer than the other.<ref>Template:Cite journal</ref>

Children with CP are prone to low trauma fractures, particularly children with higher Gross Motor Function Classification System (GMFCS) levels who cannot walk. This further affects a child's mobility, strength, and experience of pain, and can lead to missed schooling or child abuse suspicions.<ref name="Mughal2014" /> These children generally have fractures in the legs, whereas non-affected children mostly fracture their arms in the context of sporting activities.<ref>Template:Cite journal</ref>

Hip dislocation and ankle equinus or plantar flexion deformity are the two most common deformities among children with cerebral palsy. Additionally, flexion deformity of the hip and knee can occur. Torsional deformities of long bones such as the femur and tibia are also encountered, among others.<ref name="elsobky2017" /><ref name="shore2010" /> Children may develop scoliosis before the age of 10 – estimated prevalence of scoliosis in children with CP is between 21% and 64%.<ref name="Cloake2016" /> Higher levels of impairment on the GMFCS are associated with scoliosis and hip dislocation.<ref name="elsobky2017" /><ref>Template:Cite journal</ref> Scoliosis can be corrected with surgery, but CP makes surgical complications more likely, even with improved techniques.<ref name="Cloake2016" /> Hip migration can be managed by soft tissue procedures such as adductor musculature release. Advanced degrees of hip migration or dislocation can be managed by more extensive procedures such as femoral and pelvic corrective osteotomies. Both soft tissue and bony procedures aim at prevention of hip dislocation in the early phases or aim at hip containment and restoration of anatomy in the late phases of disease.<ref name="elsobky2017" /> Equinus deformity is managed by conservative methods especially when dynamic. If fixed/static deformity ensues surgery may become mandatory.<ref name="shore2010" />

Growth spurts during puberty can make walking more difficult for people with CP.<ref>Template:Cite journal</ref>

Eating[edit | edit source]

Due to sensory and motor impairments, those with CP may have difficulty preparing food, holding utensils, or chewing and swallowing. An infant with CP may not be able to suck, swallow or chew.<ref name="Klingels2010" /> Gastro-oesophageal reflux is common in children with CP.<ref name="auto" /> Children with CP may have too little or too much sensitivity around and in the mouth.<ref name="Klingels2010" /> Poor balance when sitting, lack of control of the head, mouth, and trunk, not being able to bend the hips enough to allow the arms to stretch forward to reach and grasp food or utensils, and lack of hand-eye coordination can make self-feeding difficult.<ref name="oxfordnutritionchapter" /> Feeding difficulties are related to higher GMFCS levels.<ref name="auto" /> Dental problems can also contribute to difficulties with eating.<ref name="oxfordnutritionchapter" /> Pneumonia is also common where eating difficulties exist, caused by undetected aspiration of food or liquids.<ref name="auto" /> Fine finger dexterity, like that needed for picking up a utensil, is more frequently impaired than gross manual dexterity, like that needed for spooning food onto a plate.<ref name="Donkervoort2007" />Template:Primary source inline Grip strength impairments are less common.<ref name="Donkervoort2007" />Template:Primary source inline

Children with severe cerebral palsy, particularly with oropharyngeal issues, are at risk of undernutrition.<ref>Template:Cite journal</ref> Triceps skin fold tests have been found to be a very reliable indicator of malnutrition in children with cerebral palsy.<ref name="oxfordnutritionchapter" />

Language[edit | edit source]

Speech and language disorders are common in people with cerebral palsy. The incidence of dysarthria is estimated to range from 31% to 88%,<ref name="hirsch_2013" /> and around a quarter of people with CP are non-verbal.<ref name="Myrdenetal2014" /> Speech problems are associated with poor respiratory control, laryngeal and velopharyngeal dysfunction, and oral articulation disorders that are due to restricted movement in the oral-facial muscles. There are three major types of dysarthria in cerebral palsy: spastic, dyskinetic (athetotic), and ataxic.<ref>Template:Cite book</ref>

Early use of augmentative and alternative communication systems may assist the child in developing spoken language skills.<ref name="Myrdenetal2014" /> Overall language delay is associated with problems of cognition, deafness, and learned helplessness.<ref name="CPBeuk" /> Children with cerebral palsy are at risk of learned helplessness and becoming passive communicators, initiating little communication.<ref name="CPBeuk" /> Early intervention with this clientele, and their parents, often targets situations in which children communicate with others so that they learn that they can control people and objects in their environment through this communication, including making choices, decisions, and mistakes.<ref name="CPBeuk" />

Pain and sleep[edit | edit source]

Pain is common and may result from the inherent deficits associated with the condition, along with the numerous procedures children typically face.<ref name="McKearnan_2004" /> When children with cerebral palsy are in pain, they experience worse muscle spasms.<ref>Template:Cite journal</ref> Pain is associated with tight or shortened muscles, abnormal posture, stiff joints, unsuitable orthosis, etc. Hip migration or dislocation is a recognizable source of pain in CP children and especially in the adolescent population. Nevertheless, the adequate scoring and scaling of pain in CP children remains challenging.<ref name="elsobky2017" /> Pain in CP has a number of different causes, and different pains respond to different treatments.<ref>Template:Cite journal</ref>

There is also a high likelihood of chronic sleep disorders secondary to both physical and environmental factors.<ref name="newman_2006" /> Children with cerebral palsy have significantly higher rates of sleep disturbance than typically developing children.<ref>Template:Cite journal</ref> Babies with cerebral palsy who have stiffness issues might cry more and be harder to put to sleep than non-disabled babies, or "floppy" babies might be lethargic.<ref>Template:Cite book</ref> Chronic pain is under-recognized in children with cerebral palsy,<ref>Template:Cite journal</ref> even though 3 out of 4 children with cerebral palsy experience pain.<ref>Template:Cite journal</ref> Adults with CP also experience more pain than the general population.<ref>Template:Cite journal</ref>

Associated disorders[edit | edit source]

Associated disorders include intellectual disabilities, seizures, muscle contractures, abnormal gait, osteoporosis, communication disorders, malnutrition, sleep disorders, and mental health disorders, such as depression and anxiety.<ref>Template:Cite journal</ref> In addition to these, functional gastrointestinal abnormalities contributing to bowel obstruction, vomiting, and constipation may also arise. Adults with cerebral palsy may have ischemic heart disease, cerebrovascular disease, cancer, and trauma more often.<ref>Template:Cite journal</ref> Obesity in people with cerebral palsy or a more severe Gross Motor Function Classification System assessment in particular are considered risk factors for multimorbidity.<ref>Template:Cite journal</ref> Other medical issues can be mistaken for being symptoms of cerebral palsy, and so may not be treated correctly.<ref>Template:Cite web</ref>

Related conditions can include apraxia, sensory impairments, urinary incontinence, fecal incontinence, or behavioural disorders.Template:Citation needed

Seizure management is more difficult in people with CP as seizures often last longer.<ref>Template:Cite journal</ref> Epilepsy and asthma are common co-occurring diseases in adults with CP.<ref name="The epidemiology of cerebral palsy" /> The associated disorders that co-occur with cerebral palsy may be more disabling than the motor function problems.<ref name="auto" />

Causes[edit | edit source]

File:Fetal thrombotic vasculopathy - intermed mag.jpg
Micrograph showing a fetal (placental) vein thrombosis, in a case of fetal thrombotic vasculopathy. This is associated with cerebral palsy and is suggestive of a hypercoagulable state as the underlying cause.

Cerebral palsy is due to abnormal development or damage occurring to the developing brain.<ref name="Yar2013" /> This damage can occur during pregnancy, delivery, the first month of life, or less commonly in early childhood.<ref name="Yar2013" /> Structural problems in the brain are seen in 80% of cases, most commonly within the white matter.<ref name="Yar2013" /> More than three-quarters of cases are believed to result from issues that occur during pregnancy.<ref name="Yar2013" /> Most children who are born with cerebral palsy have more than one risk factor associated with CP.<ref>Template:Cite journal</ref>

While in certain cases there is no identifiable cause, typical causes include problems in intrauterine development (e.g. exposure to radiation, infection, fetal growth restriction), hypoxia of the brain (thrombotic events, placental insufficiency, umbilical cord prolapse), birth trauma during labor and delivery, and complications around birth or during childhood.<ref name="CPBeuk" /><ref>Template:Cite journal</ref><ref name="nejm915" />

In Africa birth asphyxia, high bilirubin levels, and infections in newborns of the central nervous system are main cause. Many cases of CP in Africa could be prevented with better resources available.<ref>Template:Cite journal</ref>

Preterm birth[edit | edit source]

Between 40% and 50% of all children who develop cerebral palsy were born prematurely.<ref name="dev_beh_peds_2009" /> Most of these cases (75-90%) are believed due to issues that occur around the time of birth, often just after birth.<ref name="Yar2013" /> Multiple-birth infants are also more likely than single-birth infants to have CP.<ref name="saunders_2011" /> They are also more likely to be born with a low birth weight.Template:Citation needed

In those who are born with a weight between 1 kg and 1.5 kg CP occurs in 6%.<ref name="Osk2013" /> Among those born before 28 weeks of gestation it occurs in 8%.<ref name="Osk2016">Template:Cite journal</ref>Template:Efn Genetic factors are believed to play an important role in prematurity and cerebral palsy generally.<ref name="hallman_2012" /> While in those who are born between 34 and 37 weeks the risk is 0.4% (three times normal).<ref name="poets_2012" />

Term infants[edit | edit source]

In babies that are born at term risk factors include problems with the placenta, birth defects, low birth weight, breathing meconium into the lungs, a delivery requiring either the use of instruments or an emergency Caesarean section, birth asphyxia, seizures just after birth, respiratory distress syndrome, low blood sugar, and infections in the baby.<ref name="mcintyre_2013" />

Template:As of, it was unclear how much of a role birth asphyxia plays as a cause.<ref name="ellenberg_2013" /> It is unclear if the size of the placenta plays a role.<ref name="teng_2012" /> Template:As of it is evident that in advanced countries, most cases of cerebral palsy in term or near-term neonates have explanations other than asphyxia.<ref name="nejm915" />

Genetics[edit | edit source]

File:Autosomal recessive - en.svg
Autosomal recessive inheritance pattern.

About 2% of all CP cases are expected to be inherited, with glutamate decarboxylase-1 being one of the possible enzymes involved.<ref name="omim" /> Most inherited cases are autosomal recessive.<ref name="omim" /> However the vast majority of CP cases are connected to the brain damages created during birth and in infancy. There is a small percentage of CP cases caused by brain damages that stemmed from the prenatal period, which is estimated to be less than 5% of CP cases overall.<ref name="cdc.gov">Template:Cite web</ref> Due to that fact CP is not commonly considered a genetic disease. Moreover, there is no one reason why some CP cases come from prenatal brain damages and it's not known if those cases have a genetic basis.<ref name="cdc.gov"/>

Early childhood[edit | edit source]

After birth, other causes include toxins, severe jaundice,<ref name="cdccauses" /> lead poisoning, physical brain injury, stroke,<ref>Template:Cite web</ref> abusive head trauma, incidents involving hypoxia to the brain (such as near drowning), and encephalitis or meningitis.<ref name="cdccauses" />

Others[edit | edit source]

Infections in the mother, even those not easily detected, can triple the risk of the child developing cerebral palsy.<ref name="ucpref_2004" /> Infections of the fetal membranes known as chorioamnionitis increases the risk.<ref name="bersani_2012" />

Intrauterine and neonatal insults (many of which are infectious) increase the risk.<ref name="mwaniki_2012" />

Rh blood type incompatibility can cause the mother's immune system to attack the baby's red blood cells.<ref name="NINDS2013" />

It has been hypothesised that some cases of cerebral palsy are caused by the death in very early pregnancy of an identical twin.<ref name="pmid16354495" />

Diagnosis[edit | edit source]

The diagnosis of cerebral palsy has historically rested on the person's history and physical examination and is generally assessed at a young age. A general movements assessment, which involves measuring movements that occur spontaneously among those less than four months of age, appears most accurate.<ref name="McI2011" /><ref name="bosanquet_2013" /> Children who are more severely affected are more likely to be noticed and diagnosed earlier. Abnormal muscle tone, delayed motor development and persistence of primitive reflexes are the main early symptoms of CP.<ref name="oxfordnutritionchapter" /> Symptoms and diagnosis typically occur by the age of 2,<ref name="research gaps 2016" /> although depending on factors like malformations and congenital issues,<ref name=":1">Template:Cite web</ref> persons with milder forms of cerebral palsy may be over the age of 5, if not in adulthood, when finally diagnosed.<ref name="autogenerated1" /> Cognitive assessments and medical observations are also useful to help confirm a diagnosis. Additionally, evaluations of the child's mobility, speech and language, hearing, vision, gait, feeding and digestion are also useful to determine the extent of the disorder.<ref name=":1" /> Early diagnosis and intervention are seen as being a key part of managing cerebral palsy.<ref>Template:Cite journal</ref> Machine learning algorithms facilitate automatic early diagnosis, with methods such as deep neural network<ref>Template:Cite journal</ref> and geometric feature fusion<ref>Template:Cite journal</ref> producing high accuracy in predicting cerebral palsy from short videos. It is a developmental disability.<ref name="McI2011" />

Once a person is diagnosed with cerebral palsy, further diagnostic tests are optional. Neuroimaging with CT or MRI is warranted when the cause of a person's cerebral palsy has not been established. An MRI is preferred over CT, due to diagnostic yield and safety. When abnormal, the neuroimaging study can suggest the timing of the initial damage. The CT or MRI is also capable of revealing treatable conditions, such as hydrocephalus, porencephaly, arteriovenous malformation, subdural hematomas and hygromas, and a vermian tumour<ref name="pmid2602010" /> (which a few studies suggest are present 5–22% of the time). Furthermore, an abnormal neuroimaging study indicates a high likelihood of associated conditions, such as epilepsy and intellectual disability.<ref>Template:Cite journal</ref> There is a small risk associated with sedating children to facilitate a clear MRI.<ref name="autogenerated1" />

The age when CP is diagnosed is important, but medical professionals disagree over the best age to make the diagnosis.<ref name="bosanquet_2013" /> The earlier CP is diagnosed correctly, the better the opportunities are to provide the child with physical and educational help, but there might be a greater chance of confusing CP with another problem, especially if the child is 18 months of age or younger.<ref name="bosanquet_2013" /> Infants may have temporary problems with muscle tone or control that can be confused with CP, which is permanent.<ref name="bosanquet_2013" /> A metabolism disorder or tumors in the nervous system may appear to be CP; metabolic disorders, in particular, can produce brain problems that look like CP on an MRI.<ref name="NINDS2013" /> Disorders that deteriorate the white matter in the brain and problems that cause spasms and weakness in the legs, may be mistaken for CP if they first appear early in life.<ref name="bosanquet_2013" /> However, these disorders get worse over time, and CP does not<ref name="bosanquet_2013" /> (although it may change in character).<ref name="NINDS2013" /> In infancy it may not be possible to tell the difference between them.<ref name="bosanquet_2013" /> In the UK, not being able to sit independently by the age of 8 months is regarded as a clinical sign for further monitoring.<ref name="autogenerated1" /> Fragile X syndrome (a cause of autism and intellectual disability) and general intellectual disability must also be ruled out.<ref name="bosanquet_2013" /> Cerebral palsy specialist John McLaughlin recommends waiting until the child is 36 months of age before making a diagnosis because, by that age, motor capacity is easier to assess.<ref name="bosanquet_2013" />

Classification[edit | edit source]

CP is classified by the types of motor impairment of the limbs or organs, and by restrictions to the activities an affected person may perform.<ref name="rethlefsen_2010" /> The Gross Motor Function Classification System-Expanded and Revised and the Manual Ability Classification System are used to describe mobility and manual dexterity in people with cerebral palsy, and recently the Communication Function Classification System, and the Eating and Drinking Ability Classification System have been proposed to describe those functions.<ref name="multidisciplinary455" /> There are three main CP classifications by motor impairment: spastic, ataxic, and dyskinetic. Additionally, there is a mixed type that shows a combination of features of the other types. These classifications reflect the areas of the brain that are damaged.<ref>Template:Cite book</ref>

Cerebral palsy is also classified according to the topographic distribution of muscle spasticity.<ref name="Becher" /> This method classifies children as diplegic, (bilateral involvement with leg involvement greater than arm involvement), hemiplegic (unilateral involvement), or quadriplegic (bilateral involvement with arm involvement equal to or greater than leg involvement).<ref name="O'Shea" /><ref name="Becher" />

Spastic[edit | edit source]

Template:Main Spastic cerebral palsy is the type of cerebral palsy characterized by spasticity or high muscle tone often resulting in stiff, jerky movements.<ref name=":0:" /> Itself an umbrella term encompassing spastic hemiplegia, spastic diplegia, spastic quadriplegia and — where solely one limb or one specific area of the body is affected— spastic monoplegia. Spastic cerebral palsy affects the motor cortex<ref name=":0:" /> of the brain, a specific portion of the cerebral cortex responsible for the planning and completion of voluntary movement.<ref>Template:Cite web</ref> Spastic CP is the most common type of overall cerebral palsy, representing about 80% of cases.<ref>Template:Cite web</ref> Botulinum toxin is effective in decreasing spasticity.<ref name=Farag2020/> It can help increase range of motion which could help mitigate CPs effects on the growing bones of children.<ref name=Farag2020/> There may be an improvement in motor functions in the children and ability to walk. however, the main benefit derived from botulinum toxin A comes from its ability to reduce muscle tone and spasticity and thus prevent or delay the development of fixed muscle contractures.<ref name=Farag2020/><ref>Template:Cite journal</ref>

Ataxic[edit | edit source]

Template:Main Ataxic cerebral palsy is observed in approximately 5-10% of all cases of cerebral palsy, making it the least frequent form of cerebral palsy.<ref>Template:Cite journal</ref> Ataxic cerebral palsy is caused by damage to cerebellar structures.<ref>Template:Cite journal</ref> Because of the damage to the cerebellum, which is essential for coordinating muscle movements and balance, patients with ataxic cerebral palsy experience problems in coordination, specifically in their arms, legs, and trunk. Ataxic cerebral palsy is known to decrease muscle tone.<ref>Template:Cite journal</ref> The most common manifestation of ataxic cerebral palsy is intention (action) tremor, which is especially apparent when carrying out precise movements, such as tying shoe laces or writing with a pencil. This symptom gets progressively worse as the movement persists, making the hand shake. As the hand gets closer to accomplishing the intended task, the trembling intensifies, which makes it even more difficult to complete.<ref name="O'Shea" />

Dyskinetic[edit | edit source]

Template:Main Dyskinetic cerebral palsy (sometimes abbreviated DCP) is primarily associated with damage to the basal ganglia and the substantia nigra in the form of lesions that occur during brain development due to bilirubin encephalopathy and hypoxic-ischemic brain injury.<ref name="Hou et al" /> DCP is characterized by both hypertonia and hypotonia, due to the affected individual's inability to control muscle tone.<ref name="O'Shea" /> Clinical diagnosis of DCP typically occurs within 18 months of birth and is primarily based upon motor function and neuroimaging techniques.<ref name="ADCP" /><ref name="Mann" /> Dyskinetic cerebral palsy is an extrapyramidal form of cerebral palsy.<ref name="Jones" /> Dyskinetic cerebral palsy can be divided into two different groups; choreoathetosis and dystonia.<ref name="O'Shea" /> Choreo-athetotic CP is characterized by involuntary movements, whereas dystonic CP is characterized by slow, strong contractions, which may occur locally or encompass the whole body.<ref name="Becher" />

Mixed[edit | edit source]

Mixed cerebral palsy has symptoms of dyskinetic, ataxic and spastic CP appearing simultaneously, each to varying degrees, and both with and without symptoms of each. Mixed CP is the most difficult to treat as it is extremely heterogeneous and sometimes unpredictable in its symptoms and development over the lifespan.Template:Citation needed

Gait Classification[edit | edit source]

File:Amsterdam Gait Classification gb.jpg
The Amsterdam Gait Classification facilitates the assessment of the gait pattern in CP patients. It helps to facilitate communication in the interdisciplinary team between those affected, doctors, physiotherapists and orthotists.

In patients with spastic hemiplegia or diplegia, various gait patterns can be observed, the exact form of which can only be described with the help of complex gait analysis systems. In order to facilitate interdisciplinary communication in the interdisciplinary team between those affected, doctors, physiotherapists and orthotists, a simple description of the gait pattern is useful. J. Rodda and H. K. Graham already described in 2001 how gait patterns of CP patients can be more easily recognized and defined gait types which they compared in a classification. They also described that gait patterns can vary with age.<ref>Template:Cite journal</ref> Building on this, the Amsterdam Gait Classification was developed at the free university in Amsterdam, the VU medisch centrum. A special feature of this classification is that it makes different gait patterns very easy to recognize and can be used in CP patients in whom only one leg and both legs are affected. According to the Amsterdam Gait Classification, five gait types are described. To assess the gait pattern, the patient is viewed visually or via a video recording from the side of the leg to be assessed. At the point in time at which the leg to be viewed is in mid stance and the leg not to be viewed is in mid swing, the knee angle and the contact of the foot with the ground are assessed on the one hand.<ref name=":0">Template:Cite journal</ref>

Classification of the gait pattern according to the Amsterdam Gait Classification: In gait type 1, the knee angle is normal and the foot contact is complete. In gait type 2, the knee angle is hyperextended and the foot contact is complete. In gait type 3, the knee angle is hyperextended and foot contact is incomplete (only on the forefoot). In gait type 4, the knee angle is bent and foot contact is incomplete (only on the forefoot). With gait type 5, the knee angle is bent and the foot contact is complete.<ref name=":0" />

Gait types 5 is also known as crouch gait.Template:Citation needed

Prevention[edit | edit source]

Because the causes of CP are varied, a broad range of preventive interventions have been investigated.<ref name="Shepherd et al 2016" />

Electronic fetal monitoring has not helped to prevent CP, and in 2014 the American College of Obstetricians and Gynecologists, the Royal Australian and New Zealand College of Obstetricians and Gynaecologists, and the Society of Obstetricians and Gynaecologists of Canada have acknowledged that there are no long-term benefits of electronic fetal monitoring.<ref name="nejm915" /> Before this, electronic fetal monitoring was widely used to prop up obstetric litigation.<ref name="Sartwelle" />

In those at risk of an early delivery, magnesium sulphate appears to decrease the risk of cerebral palsy.<ref>Template:Cite journal</ref> It is unclear if it helps those who are born at term.<ref name="Ngu2013" /> In those at high risk of preterm labor a review found that moderate to severe CP was reduced by the administration of magnesium sulphate, and that adverse effects on the babies from the magnesium sulphate were not significant. Mothers who received magnesium sulphate could experience side effects such as respiratory depression and nausea.<ref>Template:Cite journal</ref> However, guidelines for the use of magnesium sulfate in mothers at risk of preterm labour are not strongly adhered to.<ref name="pmid29319155" /> Caffeine is used to treat apnea of prematurity and reduces the risk of cerebral palsy in premature babies, but there are also concerns of long term negative effects.<ref>Template:Cite journal</ref> A moderate quality level of evidence indicates that giving women antibiotics during preterm labor before her membranes have ruptured (water is not yet not broken) may increase the risk of cerebral palsy for the child.<ref name="pmid28786098" /> Additionally, for preterm babies for whom there is a chance of fetal compromise, allowing the birth to proceed rather than trying to delay the birth may lead to an increased risk of cerebral palsy in the child.<ref name="pmid28786098" /> Corticosteroids are sometimes taken by pregnant women expecting a preterm birth to provide neuroprotection to their baby.<ref>Template:Cite journal</ref> Taking corticosteroids during pregnancy is shown to have no significant correlation with developing cerebral palsy in preterm births.<ref name="pmid28786098" />

Cooling high-risk full-term babies shortly after birth may reduce disability,<ref name="jacobs_2013" /> but this may only be useful for some forms of the brain damage that causes CP.<ref name="research gaps 2016" />

Management[edit | edit source]

File:Cerebral palsy.jpg
Researchers are developing an electrical stimulation device specifically for children with cerebral palsy, who have foot drop, which causes tripping when walking.

Template:Main Over time, the approach to CP management has shifted away from narrow attempts to fix individual physical problems Template:Endash such as spasticity in a particular limb Template:Endash to making such treatments part of a larger goal of maximizing the person's independence and community engagement.<ref name="novak_2013" />Template:Rp However, the evidence base for the effectiveness of intervention programs reflecting the philosophy of independence has not yet caught up: effective interventions for body structures and functions have a strong evidence base, but evidence is lacking for effective interventions targeted toward participation, environment, or personal factors.<ref name="novak_2013" /> There is also no good evidence to show that an intervention that is effective at the body-specific level will result in an improvement at the activity level or vice versa.<ref name="novak_2013" /> Although such cross-over benefit might happen, not enough high-quality studies have been done to demonstrate it.<ref name="novak_2013" />

Because cerebral palsy has "varying severity and complexity" across the lifespan,<ref name="multidisciplinary455" /> it can be considered a collection of conditions for management purposes.<ref name="research gaps 2016" /> A multidisciplinary approach for cerebral palsy management is recommended,<ref name="multidisciplinary455" /> focusing on "maximising individual function, choice and independence" in line with the International Classification of Functioning, Disability and Health's goals.<ref name="autogenerated1" /> The team may include a paediatrician, a health visitor, a social worker, a physiotherapist, an orthotist, a speech and language therapist, an occupational therapist, a teacher specialising in helping children with visual impairment, an educational psychologist, an orthopaedic surgeon, a neurologist and a neurosurgeon.<ref>Template:Cite web</ref>

Various forms of therapy are available to people living with cerebral palsy as well as caregivers and parents. Treatment may include one or more of the following: physical therapy; occupational therapy; speech therapy; water therapy; drugs to control seizures, alleviate pain, or relax muscle spasms (e.g. benzodiazepines); surgery to correct anatomical abnormalities or release tight muscles; braces and other orthotic devices; rolling walkers; and communication aids such as computers with attached voice synthesisers.Template:Citation needed A Cochrane review published in 2004 found a trend toward the benefit of speech and language therapy for children with cerebral palsy but noted the need for high-quality research.<ref>Template:Cite journal</ref> A 2013 systematic review found that many of the therapies used to treat CP have no good evidence base; the treatments with the best evidence are medications (anticonvulsants, botulinum toxin, bisphosphonates, diazepam), therapy (bimanual training, casting, constraint-induced movement therapy, context-focused therapy, fitness training, goal-directed training, hip surveillance, home programmes, occupational therapy after botulinum toxin, pressure care) and surgery. There is also research on whether the sleeping position might improve hip migration, but there aren't yet high-quality evidence studies to support that theory.<ref>Template:Cite journal</ref> Research papers also call for an agreed consensus on outcome measures which will allow researchers to cross-reference research. Also, the terminology used to describe orthoses<ref>Template:Cite journal</ref> needs to be standardised to ensure studies can be reproduced and readily compared and evaluated. Surgical intervention in CP children mainly includes orthopaedic surgery and neurosurgery (selective dorsal rhizotomy).<ref name="Amen2018" /><ref name="novak_2013" />

Orthotics in the concept of therapy[edit | edit source]

File:Cerebralparese Orthese orthotics.jpg
Child with cerebral palsy and orthotics with adjustable functional elements to improve safety when standing and walking.

To improve the gait pattern, orthotics can be included in the therapy concept. An Orthosis can support physiotherapeutic treatment in setting the right motor impulses in order to create new cerebral connections.<ref>Template:Cite book</ref> The orthosis must meet the requirements of the medical prescription. In addition, the orthosis must be designed by the orthotist in such a way that it achieves the effectiveness of the necessary levers, matching the gait pattern, in order to support the proprioceptive approaches of physiotherapy. The characteristics of the stiffness of the orthosis shells and the adjustable dynamics in the ankle joint are important elements of the orthosis to be considered.<ref>Template:Cite book</ref> Due to these requirements, the development of orthoses has changed significantly in recent years, especially since around 2010. At about the same time, care concepts were developed that deal intensively with the orthotic treatment of the lower extremities in cerebral palsy.<ref>Template:Cite journal</ref> Modern materials and new functional elements enable the rigidity to be specifically adapted to the requirements that fits to the gait pattern of the CP patient.<ref>Template:Cite journal</ref> The adjustment of the stiffness has a decisive influence on the gait pattern and on the energy cost of walking.<ref>Template:Cite journal</ref><ref>Template:Cite journal</ref><ref>Template:Cite journal</ref> It is of great advantage if the stiffness of the orthosis can be adjusted separately from one another via resistances of the two functional elements in the two directions of movement, dorsiflexion and plantar flexion.<ref name=":5">Template:Citation</ref>

Prognosis[edit | edit source]

CP is not a progressive disorder (meaning the brain damage does not worsen), but the symptoms can become more severe over time. A person with the disorder may improve somewhat during childhood if he or she receives extensive care, but once bones and musculature become more established, orthopedic surgery may be required. People with CP can have varying degrees of cognitive impairment or none whatsoever. The full intellectual potential of a child born with CP is often not known until the child starts school. People with CP are more likely to have learning disorders but have normal intelligence. Intellectual level among people with CP varies from genius to intellectually disabled, as it does in the general population, and experts have stated that it is important not to underestimate the capabilities of a person with CP and to give them every opportunity to learn.<ref>Template:Cite journal</ref>

The ability to live independently with CP varies widely, depending partly on the severity of each person's impairment and partly on the capability of each person to self-manage the logistics of life. Some individuals with CP require personal assistant services for all activities of daily living. Others only need assistance with certain activities, and still others do not require any physical assistance. But regardless of the severity of a person's physical impairment, a person's ability to live independently often depends primarily on the person's capacity to manage the physical realities of his or her life autonomously. In some cases, people with CP recruit, hire, and manage a staff of personal care assistants (PCAs). PCAs facilitate the independence of their employers by assisting them with their daily personal needs in a way that allows them to maintain control over their lives.Template:Citation needed

Puberty in young adults with cerebral palsy may be precocious or delayed. Delayed puberty is thought to be a consequence of nutritional deficiencies.<ref name="Zaffuto-Sforza2005" /> There is currently no evidence that CP affects fertility, although some of the secondary symptoms have been shown to affect sexual desire and performance.<ref>Template:Cite journal</ref> Adults with CP were less likely to get routine reproductive health screening as of 2005. Gynecological examinations may have to be performed under anesthesia due to spasticity, and equipment is often not accessible. Breast self-examination may be difficult, so partners or carers may have to perform it. Women with CP reported higher levels of spasticity and urinary incontinence during menstruation in a study. Men with CP have higher levels of cryptorchidism at the age of 21.<ref name="Zaffuto-Sforza2005" />

CP can significantly reduce a person's life expectancy, depending on the severity of their condition and the quality of care they receive.<ref name="Yar2013" /><ref>Template:Cite journal</ref> 5-10% of children with CP die in childhood, particularly where seizures and intellectual disability also affect the child.<ref name="multidisciplinary455" /> The ability to ambulate, roll, and self-feed has been associated with increased life expectancy.<ref name="strauss_2008" /> While there is a lot of variation in how CP affects people, it has been found that "independent gross motor functional ability is a very strong determinant of life expectancy".<ref>Template:Cite journal</ref> According to the Australian Bureau of Statistics, in 2014, 104 Australians died of cerebral palsy.<ref>Template:Cite web</ref> The most common causes of death in CP are related to respiratory causes, but in middle age cardiovascular issues and neoplastic disorders become more prominent.<ref name="rehabilitation443" />

Self-care[edit | edit source]

For many children with CP, parents are heavily involved in self-care activities. Self-care activities, such as bathing, dressing, and grooming, can be difficult for children with CP, as self-care depends primarily on the use of the upper limbs.<ref name="vanzelst_2006" /> For those living with CP, impaired upper limb function affects almost 50% of children and is considered the main factor contributing to decreased activity and participation.<ref name="Nieuwenhuijsen_2009" /> As the hands are used for many self-care tasks, sensory and motor impairments of the hands make daily self-care more difficult.<ref name="Donkervoort2007" />Template:Primary source inline<ref name="arnould_2008" /> Motor impairments cause more problems than sensory impairments.<ref name="Donkervoort2007" /> The most common impairment is that of finger dexterity, which is the ability to manipulate small objects with the fingers.<ref name="Donkervoort2007" /> Compared to other disabilities, people with cerebral palsy generally need more help in performing daily tasks.<ref>Template:Cite web Disability Series. Cat. no. DIS 49. Canberra: AIHW.</ref> Occupational therapists are healthcare professionals that help individuals with disabilities gain or regain their independence through the use of meaningful activities.<ref>Template:Cite web</ref>

Productivity[edit | edit source]

The effects of sensory, motor, and cognitive impairments affect self-care occupations in children with CP and productivity occupations. Productivity can include but is not limited to, school, work, household chores, or contributing to the community.<ref name="fedrizzi_2003" />

Play is included as a productive occupation as it is often the primary activity for children.<ref name="Blesedell CE 2003. p. 705-709" /> If play becomes difficult due to a disability, like CP, this can cause problems for the child.<ref name="Townsend E 2002. p. 34" /> These difficulties can affect a child's self-esteem.<ref name="Townsend E 2002. p. 34" /> In addition, the sensory and motor problems experienced by children with CP affect how the child interacts with their surroundings, including the environment and other people.<ref name="Townsend E 2002. p. 34" /> Not only do physical limitations affect a child's ability to play, the limitations perceived by the child's caregivers and playmates also affect the child's play activities.<ref name="parham_1997" /> Some children with disabilities spend more time playing by themselves.<ref name="miller_2003" /> When a disability prevents a child from playing, there may be social, emotional and psychological problems,<ref name="okimoto_2000" /> which can lead to increased dependence on others, less motivation, and poor social skills.<ref name="hestenes_2000" />

In school, students are asked to complete many tasks and activities, many of which involve handwriting. Many children with CP have the capacity to learn and write in the school environment.<ref name="Missiuna" /> However, students with CP may find it difficult to keep up with the handwriting demands of school and their writing may be difficult to read.<ref name="Missiuna" /> In addition, writing may take longer and require greater effort on the student's part.<ref name="Missiuna" /> Factors linked to handwriting include postural stability, sensory and perceptual abilities of the hand, and writing tool pressure.<ref name="Missiuna" />

Speech impairments may be seen in children with CP depending on the severity of brain damage.<ref name="howard_1996" /> Communication in a school setting is important because communicating with peers and teachers is very much a part of the "school experience" and enhances social interaction. Problems with language or motor dysfunction can lead to underestimating a student's intelligence.<ref name="rigby_1999" /> In summary, children with CP may experience difficulties in school, such as difficulty with handwriting, carrying out school activities, communicating verbally, and interacting socially.Template:Citation needed

Leisure[edit | edit source]

Leisure activities can have several positive effects on physical health, mental health, life satisfaction, and psychological growth for people with physical disabilities like CP.<ref name="smith_2009" /> Common benefits identified are stress reduction, development of coping skills, companionship, enjoyment, relaxation and a positive effect on life satisfaction.<ref name="ReferenceC" /> In addition, for children with CP, leisure appears to enhance adjustment to living with a disability.<ref name="ReferenceC" />

Leisure can be divided into structured (formal) and unstructured (informal) activities.<ref name="cassidy_1996" /> Children and teens with CP engage in less habitual physical activity than their peers.<ref>Template:Cite journal</ref> Children with CP primarily engage in physical activity through therapies aimed at managing their CP, or through organized sport for people with disabilities.<ref>Template:Cite journal</ref> It is difficult to sustain behavioural change in terms of increasing physical activity of children with CP.<ref>Template:Cite journal Template:Open access</ref> Gender, manual dexterity, the child's preferences, cognitive impairment and epilepsy were found to affect children's leisure activities, with manual dexterity associated with more leisure activity.<ref>Template:Cite journal</ref> Although leisure is important for children with CP, they may have difficulties carrying out leisure activities due to social and physical barriers.Template:Citation needed

Children with cerebral palsy may face challenges when it comes to participating in sports. This comes with being discouraged from physical activity because of these perceived limitations imposed by their medical condition.<ref>Template:Cite journal</ref>

Participation and barriers[edit | edit source]

Participation is involvement in life situations and everyday activities.<ref name="King" /> Participation includes self-care, productivity, and leisure. In fact, communication, mobility, education, home life, leisure, and social relationships require participation, and indicate the extent to which children function in their environment.<ref name="King" /> Barriers can exist on three levels: micro, meso, and macro.<ref name="Aitchison" /> First, the barriers at the micro level involve the person.<ref name="Aitchison" /> Barriers at the micro level include the child's physical limitations (motor, sensory and cognitive impairments) or their subjective feelings regarding their ability to participate.<ref name="imms_2008" /> For example, the child may not participate in group activities due to lack of confidence. Second, barriers at the meso level include the family and community.<ref name="Aitchison" /> These may include negative attitudes of people toward disability or lack of support within the family or in the community.<ref name="Specht" /> One of the main reasons for this limited support appears to be the result of a lack of awareness and knowledge regarding the child's ability to engage in activities despite his or her disability.<ref name="Specht" /> Third, barriers at the macro level incorporate the systems and policies that are not in place or hinder children with CP. These may be environmental barriers to participation such as architectural barriers, lack of relevant assistive technology, and transportation difficulties due to limited wheelchair access or public transit that can accommodate children with CP.<ref name="Specht" /> For example, a building without an elevator can prevent the child from accessing higher floors.Template:Citation needed

A 2013 review stated that outcomes for adults with cerebral palsy without intellectual disability in the 2000s were that "60–80% completed high school, 14–25% completed college, up to 61% were living independently in the community, 25–55% were competitively employed, and 14–28% were involved in long term relationships with partners or had established families".<ref>Template:Cite journal</ref> Adults with cerebral palsy may not seek physical therapy due to transport issues, financial restrictions and practitioners not feeling like they know enough about cerebral palsy to take people with CP on as clients.<ref name="Lawrence2016" />

A study in young adults (18–34) on transitioning to adulthood found that their concerns were physical health care and understanding their bodies, being able to navigate and use services and supports successfully, and dealing with prejudices. A feeling of being "thrust into adulthood" was common in the study.<ref>Template:Cite journal</ref>

Aging[edit | edit source]

Children with CP may not successfully transition into using adult services because they are not referred to one upon turning 18, and may decrease their use of services.<ref name="rehabilitation443" /> Because children with cerebral palsy are often told that it is a non-progressive disease, they may be unprepared for the greater effects of the aging process as they head into their 30s.<ref>Turk, M.A., Overeynder, J.C., & Janicki, M.P. (Eds.). (1995). Uncertain Future – Aging and Cerebral Palsy: Clinical Concerns. Albany: New York State Developmental Disabilities Planning Council. Template:Webarchive</ref> Young adults with cerebral palsy experience problems with aging that able-bodied adults experience "much later in life".<ref name="Kerkovich, D 2009, pp. 41-53" />Template:Rp 25% or more adults with cerebral palsy who can walk experience increasing difficulties walking with age.<ref>Template:Cite journal</ref> Hand function does not seem to have similar declines.<ref name="The epidemiology of cerebral palsy" /> Chronic disease risk, such as obesity, is also higher among adults with cerebral palsy than the general population.<ref>Template:Cite journal</ref> Common problems include increased pain, reduced flexibility, increased spasms and contractures, post-impairment syndrome<ref>Template:Cite web</ref> and increasing problems with balance.<ref name="hirsch_2013" /> Increased fatigue is also a problem.<ref name="Developmental Medicine 2011" /> When adulthood and cerebral palsy is discussed, Template:As of, it is not discussed in terms of the different stages of adulthood.<ref name="Developmental Medicine 2011" />

Like they did in childhood, adults with cerebral palsy experience psychosocial issues related to their CP, chiefly the need for social support, self-acceptance, and acceptance by others. Workplace accommodations may be needed to enhance continued employment for adults with CP as they age. Rehabilitation or social programs that include salutogenesis may improve the coping potential of adults with CP as they age.<ref>Template:Cite journal</ref>

Epidemiology[edit | edit source]

Cerebral palsy occurs in about 2.1 per 1000 live births.<ref name="Osk2013" /> In those born at term rates are lower at 1 per 1000 live births.<ref name="Yar2013" /> Rates appear to be similar in both the developing and developed world.<ref name="Yar2013" /> Within a population it may occur more often in poorer people.<ref>Template:Cite journal</ref> The rate is higher in males than in females; in Europe it is 1.3 times more common in males.<ref name="JohnsonPrevalence" />

There was a "moderate, but significant" rise in the prevalence of CP between the 1970s and 1990s. This is thought to be due to a rise in low birth weight of infants and the increased survival rate of these infants. The increased survival rate of infants with CP in the 1970s and 80s may be indirectly due to the disability rights movement challenging perspectives around the worth of infants with a disability, as well as the Baby Doe Law.<ref>Template:Cite journal</ref>

As of 2005, advances in the care of pregnant mothers and their babies have not resulted in a noticeable decrease in CP. This is generally attributed to medical advances in areas related to the care of premature babies (which results in a greater survival rate). Only the introduction of quality medical care to locations with less-than-adequate medical care has shown any decreases. The incidence of CP increases with premature or very low-weight babies regardless of the quality of care.<ref name="bax_2005" /> Template:As of, there is a suggestion that both incidence and severity are slightly decreasing – more research is needed to find out if this is significant, and if so, which interventions are effective.<ref name="Shepherd et al 2016" />

Prevalence of cerebral palsy is best calculated around the school entry age of about 6 years, the prevalence in the U.S. is estimated to be 2.4 out of 1000 children.<ref name="pmid17261678" />

History[edit | edit source]

Cerebral palsy has affected humans since antiquity. A decorated grave marker dating from around the 15th to 14th century BCE shows a figure with one small leg and using a crutch, possibly due to cerebral palsy. The oldest likely physical evidence of the condition comes from the mummy of Siptah, an Egyptian Pharaoh who ruled from about 1196 to 1190 BCE and died at about 20 years of age. The presence of cerebral palsy has been suspected due to his deformed foot and hands.<ref name="History2013" />

The medical literature of the ancient Greeks discusses paralysis and weakness of the arms and legs; the modern word palsy comes from the Ancient Greek words παράλυση or πάρεση, meaning paralysis or paresis respectively. The works of the school of Hippocrates (460Template:Endashc. 370 BCE), and the manuscript On the Sacred Disease in particular, describe a group of problems that matches up very well with the modern understanding of cerebral palsy. The Roman Emperor Claudius (10 BCETemplate:Endash54 CE) is suspected of having CP, as historical records describe him as having several physical problems in line with the condition. Medical historians have begun to suspect and find depictions of CP in much later art. Several paintings from the 16th century and later show individuals with problems consistent with it, such as Jusepe de Ribera's 1642 painting The Clubfoot.<ref name="History2013" />

The modern understanding of CP as resulting from problems within the brain began in the early decades of the 1800s with a number of publications on brain abnormalities by Johann Christian Reil, Claude François Lallemand and Philippe Pinel. Later physicians used this research to connect problems in the brain with specific symptoms. The English surgeon William John Little (1810Template:Endash1894) was the first person to study CP extensively. In his doctoral thesis he stated that CP was a result of a problem around the time of birth. He later identified a difficult delivery, a preterm birth and perinatal asphyxia in particular as risk factors. The spastic diplegia form of CP came to be known as Little's disease.<ref name="History2013" /> At around this time, a German surgeon was also working on cerebral palsy, and distinguished it from polio.<ref>Template:Cite journal</ref> In the 1880s British neurologist William Gowers built on Little's work by linking paralysis in newborns to difficult births. He named the problem "birth palsy" and classified birth palsies into two types: peripheral and cerebral.<ref name="History2013" />

Working in Pennsylvania in the 1880s, Canadian-born physician William Osler (1849Template:Endash1919) reviewed dozens of CP cases to further classify the disorders by the site of the problems on the body and by the underlying cause. Osler made further observations tying problems around the time of delivery with CP, and concluded that problems causing bleeding inside the brain were likely the root cause. Osler also suspected polioencephalitis as an infectious cause. Through the 1890s, scientists commonly confused CP with polio.<ref name="History2013" />

Before moving to psychiatry, Austrian neurologist Sigmund Freud (1856Template:Endash1939) made further refinements to the classification of the disorder. He produced the system still being used today. Freud's system divides the causes of the disorder into problems present at birth, problems that develop during birth, and problems after birth. Freud also made a rough correlation between the location of the problem inside the brain and the location of the affected limbs on the body and documented the many kinds of movement disorders.<ref name="History2013" />

In the early 20th century, the attention of the medical community generally turned away from CP until orthopedic surgeon Winthrop Phelps became the first physician to treat the disorder. He viewed CP from a musculoskeletal perspective instead of a neurological one. Phelps developed surgical techniques for operating on the muscles to address issues such as spasticity and muscle rigidity. Hungarian physical rehabilitation practitioner András Pető developed a system to teach children with CP how to walk and perform other basic movements. Pető's system became the foundation for conductive education, widely used for children with CP today. Through the remaining decades, physical therapy for CP has evolved, and has become a core component of the CP management program.<ref name="History2013" />

In 1997, Robert Palisano et al. introduced the Gross Motor Function Classification System (GMFCS) as an improvement over the previous rough assessment of limitation as either mild, moderate, or severe.<ref name="rethlefsen_2010" /> The GMFCS grades limitation based on observed proficiency in specific basic mobility skills such as sitting, standing, and walking, and takes into account the level of dependency on aids such as wheelchairs or walkers. The GMFCS was further revised and expanded in 2007.<ref name="rethlefsen_2010" />

Society and culture[edit | edit source]

Economic impact[edit | edit source]

It is difficult to directly compare the cost and cost-effectiveness of interventions to prevent cerebral palsy or the cost of interventions to manage CP.<ref name="pmid29319155" /> Access Economics has released a report on the economic impact of cerebral palsy in Australia. The report found that, in 2007, the financial cost of cerebral palsy (CP) in Australia was A$1.47 billion or 0.14% of GDP.<ref name="spasticcentre" /> Of this:

  • A$1.03 billion (69.9%) was productivity lost due to lower employment, absenteeism, and premature death of Australians with CP
  • A$141 million (9.6%) was the DWL from transfers including welfare payments and taxation forgone
  • A$131 million (9.0%) was other indirect costs such as direct program services, aides and home modifications, and the bringing-forward of funeral costs
  • A$129 million (8.8%) was the value of the informal care for people with CP
  • A$40 million (2.8%) was direct health system expenditure

The value of lost well-being (disability and premature death) was a further A$2.4 billion.Template:Citation needed

In per capita terms, this amounts to a financial cost of A$43,431 per person with CP per annum. Including the value of lost well-being, the cost is over $115,000 per person per annum.Template:Citation needed

Individuals with CP bear 37% of the financial costs, and their families and friends bear a further 6%. The federal government bears around one-third (33%) of the financial costs (mainly through taxation revenues forgone and welfare payments). State governments bear under 1% of the costs, while employers bear 5% and the rest of society bears the remaining 19%. If the burden of disease (lost well-being) is included, individuals bear 76% of the costs.Template:Citation needed

The average lifetime cost for people with CP in the US is US$921,000 per individual, including lost income.<ref name="pmid14749614" />

In the United States, many states allow Medicaid beneficiaries to use their Medicaid funds to hire their own PCAs, instead of forcing them to use institutional or managed care.<ref name="medicaid" />

In India, the government-sponsored program called "NIRAMAYA" for the medical care of children with neurological and muscular deformities has proved to be an ameliorating economic measure for persons with such disabilities.<ref>Template:Cite web</ref> It has shown that persons with mental or physically debilitating congenital disabilities can lead better lives if they have financial independence.<ref>Template:Cite news</ref>

Use of the term[edit | edit source]

"Cerebral" means "of, or pertaining to, the cerebrum or the brain"<ref>Template:Cite web</ref> and "palsy" means "paralysis, generally partial, whereby a local body area is incapable of voluntary movement".<ref>Template:Cite web</ref> It has been proposed to change the name to "cerebral palsy spectrum disorder" to reflect the diversity of presentations of CP.<ref>Template:Cite journal</ref>

Many people would rather be referred to as a person with a disability (people-first language) instead of as "handicapped". "Cerebral Palsy: A Guide for Care" at the University of Delaware offers the following guidelines:

Template:Blockquote

The term "spastic" denotes the attribute of spasticity in types of spastic CP. In 1952 a UK charity called The Spastics Society was formed.<ref name="Guardian20020522" /> The term "spastics" was used by the charity as a term for people with CP. The word "spastic" has since been used extensively as a general insult to disabled people, which some see as extremely offensive. They are also frequently used to insult able-bodied people when they seem overly uncoordinated, anxious, or unskilled in sports. The charity changed its name to Scope in 1994.<ref name="Guardian20020522" /> In the United States the word spaz has the same usage as an insult but is not generally associated with CP.<ref name="zimmer" />

Media[edit | edit source]

Template:See also

Maverick documentary filmmaker Kazuo Hara criticises the mores and customs of Japanese society in an unsentimental portrait of adults with cerebral palsy in his 1972 film Goodbye CP (Sayonara CP). Focusing on how people with cerebral palsy are generally ignored or disregarded in Japan, Hara challenges his society's taboos about physical handicaps. Using a deliberately harsh style, with grainy black-and-white photography and out-of-sync sound, Hara brings a stark realism to his subject.<ref name="dvdtalk" />

Spandan (2012), a film by Vegitha Reddy and Aman Tripathi, delves into the dilemma of parents whose child has cerebral palsy. While films made with children with special needs as central characters have been attempted before, the predicament of parents dealing with the stigma associated with the condition and beyond is dealt in Spandan. In one of the songs of Spandan "Chal chaal chaal tu bala" more than 50 CP kids have acted. The famous classical singer Devaki Pandit has given her voice to the song penned by Prof. Jayant Dhupkar and composed by National Film Awards winner Isaac Thomas Kottukapally.<ref name="hindu" /><ref name="hindu2" /><ref name="newsleaks" /><ref name="deccan" />

My Left Foot (1989) is a drama film directed by Jim Sheridan and starring Daniel Day-Lewis. It tells the true story of Christy Brown, an Irishman born with cerebral palsy, who could control only his left foot. Christy Brown grew up in a poor, working-class family, and became a writer and artist. It won the Academy Award for Best Actor (Daniel Day-Lewis) and Best Actress in a Supporting Role (Brenda Fricker). It was also nominated for Best Director, Best Picture and Best Writing, Screenplay Based on Material from Another Medium. It also won the New York Film Critics Circle Award for Best Film for 1989.<ref name="latimes" />

Call the Midwife (2012–) has featured two episodes with actor Colin Young, who himself has cerebral palsy, playing a character with the same disability. His storylines have focused on the segregation of those with disabilities in the UK in the 1950s, and also romantic relationships between people with disabilities.<ref>Template:Cite web</ref>

Micah Fowler, an American actor with CP, stars in the ABC sitcom Speechless (2016–19), which explores both the serious and humorous challenges a family faces with a teenager with CP.<ref>Template:Cite news</ref>

Special (2019) is a comedy series that premiered on Netflix on 12 April 2019. It was written, produced and stars Ryan O'Connell as a young gay man with mild cerebral palsy. It is based on O'Connell's book I'm Special: And Other Lies We Tell Ourselves.<ref>Template:Cite news</ref>

Australian drama serial The Heights (2019–) features a character with mild cerebral palsy, teenage girl Sabine Rosso, depicted by an actor who herself has mild cerebral palsy, Bridie McKim.<ref>Template:Cite news</ref>

Notable cases[edit | edit source]

Template:Category see also

Litigation[edit | edit source]

Because of the false perception that cerebral palsy is mostly caused by trauma during birth, as of 2005, 60% of obstetric litigation was about cerebral palsy, which Alastair MacLennan, Professor of Obstetrics and Gynaecology at the University of Adelaide, regards as causing an exodus from the profession.<ref>Template:Cite news</ref> In the latter half of the 20th century, obstetric litigation about the cause of cerebral palsy became more common, leading to the practice of defensive medicine.<ref name="Sartwelle" />

See also[edit | edit source]

Notes[edit | edit source]

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References[edit | edit source]

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