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Results 1 - 10 of 286 for Brain atrophy
  1. ... images of what the eye sees to the brain. ... can also cause a form of optic nerve atrophy. The condition can also be caused by diseases of the brain and central nervous system. These may include: Brain ...
  2. ... 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 ...
  3. ... RA. CLPB mutations cause 3-methylglutaconic aciduria, progressive brain atrophy, intellectual disability, congenital neutropenia, cataracts, movement disorder. Am ...
  4. ... RA. CLPB mutations cause 3-methylglutaconic aciduria, progressive brain atrophy, intellectual disability, congenital neutropenia, cataracts, movement disorder. Am ...
  5. ... leading to an overall loss of brain tissue (brain atrophy) and an unusually small head (microcephaly). Children with ...
  6. Dementias From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Dementia/Start Here ... Dementia ... Lewy Body Dementia/Statistics and Research ... Lewy Body Dementia ... National Institute of Neurological Disorders and Stroke ... Dementia ...
  7. ... of myelin and disrupting nerve signaling in the brain. Degeneration (atrophy) of brain tissue caused by excess lipid deposits also contributes ...
  8. Parry-Romberg Syndrome From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Mouth Disorders/Related Issues ... Mouth Disorders ... Facial Injuries and Disorders/Specifics ... Facial Injuries and Disorders ... National Institute of Neurological Disorders ...
  9. Juvenile Onset HD (Huntington's Disease Society of America) - PDF  
    What Is Juvenile Onset Huntington's Disease (JHD)? Juvenile Onset Huntington's Disease (JHD) is a form of Huntington's disease (HD) that affects children ...
  10. ... 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: ...
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