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Results 1 - 10 of 127 for Brain atrophy
  1. Phosphoglycerate dehydrogenase deficiency 
    ... cells leading to a loss of brain tissue (brain atrophy), specifically affecting the fatty tissue known as myelin that surrounds nerve cells (hypomyelination). Frequently, the tissue that connects the two halves of the brain (corpus callosum) is small and thin, and the ...
    https://medlineplus.gov/...phosphoglycerate-dehydrogenase-deficiency - Genetics
  2. CLPB gene 
    ... RA. CLPB mutations cause 3-methylglutaconic aciduria, progressive brain atrophy, intellectual disability, congenital neutropenia, cataracts, movement disorder. Am ...
    https://medlineplus.gov/genetics/gene/clpb - Genetics
  3. CLPB deficiency 
    ... RA. CLPB mutations cause 3-methylglutaconic aciduria, progressive brain atrophy, intellectual disability, congenital neutropenia, cataracts, movement disorder. Am ...
    https://medlineplus.gov/genetics/condition/clpb-deficiency - Genetics
  4. CLN1 disease 
    ... leading to an overall loss of brain tissue (brain atrophy) and an unusually small head (microcephaly). Children with ...
    https://medlineplus.gov/genetics/condition/cln1-disease - Genetics
  5. Cerebrotendinous xanthomatosis 
    ... of myelin and disrupting nerve signaling in the brain. Degeneration (atrophy) of brain tissue caused by excess lipid deposits also contributes ...
    https://medlineplus.gov/.../condition/cerebrotendinous-xanthomatosis - Genetics
  6. OPA1 gene 
    ... early childhood. Individuals with Behr syndrome develop optic atrophy, brain dysfunction (encephalopathy), loss of sensation and weakness in ... OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes. Brain. 2008 Feb;131(Pt 2):338-51. doi: ...
    https://medlineplus.gov/genetics/gene/opa1 - Genetics
  7. Sturge-Weber syndrome 
    ... in the brain and lead to loss of brain tissue (atrophy) and deposits of calcium (calcification) in the brain below the angioma. The decrease in blood flow ...
    https://medlineplus.gov/genetics/condition/sturge-weber-syndrome - Genetics
  8. TUBB4A-related leukodystrophy 
    ... In addition, tissue in certain regions of the brain breaks down (atrophies), most prominently in a region called the putamen, ... structures that help control movement (the basal ganglia). Atrophy of brain tissue in another region involved in movement called ...
    https://medlineplus.gov/.../condition/tubb4a-related-leukodystrophy - Genetics
  9. CISD2 gene 
    ... that carry information from the eyes to the brain (optic atrophy), and a number of other features involving the urinary tract, the brain, and hearing. People with this CISD2 gene mutation ...
    https://medlineplus.gov/genetics/gene/cisd2 - Genetics
  10. WFS1 gene 
    ... that carry information from the eyes to the brain (optic atrophy), and a number of other features involving the urinary tract, the brain, and hearing. Typically, variants in both copies of ...
    https://medlineplus.gov/genetics/gene/wfs1 - Genetics
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