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Results 1 - 6 of 6 for Neurodevelopmental disorder with seizures brain atrophy
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  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 
    ... In about one-quarter of affected individuals, the seizures are described as ... The prevalence ...
    https://medlineplus.gov/genetics/condition/stxbp1-encephalopathy - Genetics
  3. Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart 
    Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart (NEDBEH) is a neurological disorder that can also affect many other body systems. This ...
    https://medlineplus.gov/...thout-anomalies-of-the-brain-eye-or-heart - Genetics
  4. 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
  5. CHD2 myoclonic encephalopathy 
    ... people with CHD2 myoclonic encephalopathy have autism spectrum disorders, which are conditions characterized by impaired communication and social interaction. In some instances, areas with a loss of brain tissue (atrophy) have been found with medical imaging. The prevalence ...
    https://medlineplus.gov/.../condition/chd2-myoclonic-encephalopathy - Genetics
  6. Peroxisomal acyl-CoA oxidase deficiency 
    Peroxisomal acyl-CoA oxidase deficiency ... eyes (hypertelorism), a low nasal bridge, and low-set ears. Extra fingers or toes ( ...
    https://medlineplus.gov/.../peroxisomal-acyl-coa-oxidase-deficiency - Genetics