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Results 1 - 6 of 6 for Neurodevelopmental disorder with epilepsy brain atrophy
  1. DLG4-related synaptopathy 
    ... this condition cannot speak. Affected individuals often have ... tissue loss (atrophy) and abnormalities of the tissue connecting the left ...
    https://medlineplus.gov/genetics/condition/dlg4-related-synaptopathy - Genetics
  2. STXBP1 encephalopathy 
    ... JR, Moller RS, Weckhuysen S. STXBP1 encephalopathy: A neurodevelopmental ... patients with epileptic encephalopathy. Brain Dev. 2016 Mar;38(3):280-4. doi: ...
    https://medlineplus.gov/genetics/condition/stxbp1-encephalopathy - Genetics
  3. CHD2 myoclonic encephalopathy 
    ... acquired skills (developmental regression) following the onset of epilepsy. Some people ... The prevalence ...
    https://medlineplus.gov/.../condition/chd2-myoclonic-encephalopathy - Genetics
  4. Genetic Brain Disorders (National Library of Medicine)  
    A genetic brain disorder is caused by a variation or a mutation in a gene. A variation is a different form of a gene. A mutation is a change in a gene. ...
    https://medlineplus.gov/geneticbraindisorders.html - Health Topics
  5. ATN1 gene 
    ... gene ranges from 6 to 35. Dentatorubral-pallidoluysian atrophy (DRPLA) is a progressive brain disorder that causes involuntary movements, mental and emotional problems, ...
    https://medlineplus.gov/genetics/gene/atn1 - Genetics
  6. Peroxisomal acyl-CoA oxidase deficiency 
    ... muscle tone (hypertonia), more severe and recurrent seizures (epilepsy), and loss of vision and ... acyl-CoA oxidase deficiency is a rare disorder. Its prevalence is unknown. Only a few dozen ...
    https://medlineplus.gov/.../peroxisomal-acyl-coa-oxidase-deficiency - Genetics