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Results 1 - 10 of 15 for "Encephalopathy," "recurrent," of childhood
  1. 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
  2. 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
  3. 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
  4. 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
  5. GABA-transaminase deficiency 
    GABA-transaminase deficiency is a brain disease ... GABA- ...
    https://medlineplus.gov/.../condition/gaba-transaminase-deficiency - Genetics
  6. Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes 
    ... symptoms of this disorder most often appear in childhood following a period of normal ... encephalopathy, lactic acidosis, and stroke-like episodes Mitochondrial myopathy, ...
    https://medlineplus.gov/...-lactic-acidosis-and-stroke-like-episodes - Genetics
  7. 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
  8. Asparagine synthetase deficiency 
    ... legs (spastic quadriplegia). Many affected individuals also have recurrent seizures ... ...
    https://medlineplus.gov/.../asparagine-synthetase-deficiency - Genetics
  9. Genetic epilepsy with febrile seizures plus 
    Genetic epilepsy with febrile seizures plus (GEFS+) is a spectrum of seizure disorders of varying severity. GEFS+ is usually diagnosed in families whose members ...
    https://medlineplus.gov/...netic-epilepsy-with-febrile-seizures-plus - Genetics
  10. Malignant migrating partial seizures of infancy 
    ... individuals do not survive past infancy or early childhood. ... T, Osawa M, Hirose S, Yamamoto T. A recurrent KCNT1 mutation in two sporadic cases with malignant ...
    https://medlineplus.gov/...ant-migrating-partial-seizures-of-infancy - Genetics
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