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Results 1 - 10 of 48 for Recurrent encephalopathy
  1. KCNB1 encephalopathy 
    ... is a condition characterized by abnormal brain function (encephalopathy), recurrent seizures (epilepsy), and developmental delay.Most people who have KCNB1 encephalopathy have more than one type of seizure. The ...
    https://medlineplus.gov/genetics/condition/kcnb1-encephalopathy - Genetics
  2. SCN8A-related epilepsy with encephalopathy 
    ... epilepsy with encephalopathy is a condition characterized by recurrent seizures (epilepsy), abnormal brain function (encephalopathy), and intellectual disability. The signs and symptoms of ...
    https://medlineplus.gov/...cn8a-related-epilepsy-with-encephalopathy - Genetics
  3. 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 ...
    https://medlineplus.gov/.../condition/chd2-myoclonic-encephalopathy - Genetics
  4. Acute necrotizing encephalopathy type 1 
    ... response play a role in individuals' susceptibility to recurrent episodes of acute necrotizing encephalopathy type 1. In people with acute necrotizing encephalopathy ...
    https://medlineplus.gov/.../acute-necrotizing-encephalopathy-type-1 - Genetics
  5. RANBP2 gene 
    ... response play a role in individuals' susceptibility to recurrent episodes of acute necrotizing encephalopathy type 1. In people with acute necrotizing encephalopathy ...
    https://medlineplus.gov/genetics/gene/ranbp2 - Genetics
  6. Mitochondrial complex I deficiency 
    ... have neurological problems, such as abnormal brain function (encephalopathy), recurrent seizures (epilepsy), intellectual disability, difficulty coordinating movements (ataxia), ...
    https://medlineplus.gov/.../mitochondrial-complex-i-deficiency - Genetics
  7. KCNB1 gene 
    ... This condition is characterized by abnormal brain function (encephalopathy), recurrent seizures (epilepsy), and developmental delay.Most KCNB1 gene ...
    https://medlineplus.gov/genetics/gene/kcnb1 - Genetics
  8. SCN8A gene 
    ... epilepsy with encephalopathy. This condition is characterized by recurrent seizures (epilepsy), abnormal brain function (encephalopathy), and intellectual disability. The signs and symptoms of ...
    https://medlineplus.gov/genetics/gene/scn8a - Genetics
  9. 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 ...
    https://medlineplus.gov/genetics/gene/chd2 - Genetics
  10. SLC19A3 gene 
    ... responsive basal ganglia disease, a disorder that involves recurrent episodes of brain dysfunction (encephalopathy) and a variety of neurological problems that gradually ...
    https://medlineplus.gov/genetics/gene/slc19a3 - Genetics
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