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Results 1 - 10 of 25 for "Encephalopathy," "recurrent," of childhood
  1. CHD2 gene 
    ... cause CHD2 myoclonic encephalopathy, a condition characterized by recurrent seizures (epilepsy), abnormal brain function (encephalopathy), and intellectual disability beginning in childhood. About half of these mutations delete pieces of ...
    https://medlineplus.gov/genetics/gene/chd2 - Genetics
  2. CHD2 myoclonic encephalopathy 
    CHD2 myoclonic encephalopathy is a condition characterized by recurrent seizures (epilepsy), abnormal brain function (encephalopathy), and intellectual disability. Epilepsy begins in childhood, typically between ages 6 months and 4 years. ...
    https://medlineplus.gov/.../condition/chd2-myoclonic-encephalopathy - Genetics
  3. STXBP1 encephalopathy 
    ... is a condition characterized by abnormal brain function (encephalopathy) and ... later in childhood or early adulthood. In many affected individuals who ...
    https://medlineplus.gov/genetics/condition/stxbp1-encephalopathy - Genetics
  4. Infantile-onset spinocerebellar ataxia 
    ... nerve damage (sensorineural hearing loss) typically occurs during childhood and progresses to profound deafness.Individuals with IOSCA may have recurrent seizures (epilepsy). These seizures can lead to severe brain dysfunction (encephalopathy).Most people with IOSCA survive into adulthood. However, ...
    https://medlineplus.gov/.../infantile-onset-spinocerebellar-ataxia - Genetics
  5. Epilepsy-aphasia spectrum 
    ... Many people with conditions in this spectrum develop recurrent seizures ... encephalopathy with continuous spike-and-wave during sleep syndrome ( ...
    https://medlineplus.gov/genetics/condition/epilepsy-aphasia-spectrum - Genetics
  6. GRIN2A gene 
    ... sometimes other developmental skills; and in many cases, recurrent seizures ... while childhood epilepsy with centrotemporal spikes (CECTS) is at the ...
    https://medlineplus.gov/genetics/gene/grin2a - Genetics
  7. ABAT gene 
    ... GABA-transaminase deficiency, which is a brain disease (encephalopathy) ... longer into childhood.The ABAT gene mutations that cause GABA-transaminase ...
    https://medlineplus.gov/genetics/gene/abat - Genetics
  8. GABA-transaminase deficiency 
    GABA-transaminase deficiency is a brain disease ... GABA- ...
    https://medlineplus.gov/.../condition/gaba-transaminase-deficiency - Genetics
  9. Beta-propeller protein-associated neurodegeneration 
    ... instability), and a shuffling walk that can cause recurrent falls.The lifespan of ... Genetic Testing Registry: Neurodegeneration ...
    https://medlineplus.gov/...ller-protein-associated-neurodegeneration - Genetics
  10. Asparagine synthetase deficiency 
    ... legs (spastic quadriplegia). Many affected individuals also have recurrent seizures ... ...
    https://medlineplus.gov/.../asparagine-synthetase-deficiency - Genetics
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