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Results 1 - 10 of 12 for Cerebral white matter atrophy
  1. 3-methylglutaconyl-CoA hydratase deficiency 
    ... These individuals have damage to a type of brain tissue called white matter ... optic atrophy, and a decline in intellectual function (dementia).Affected ...
    https://medlineplus.gov/...methylglutaconyl-coa-hydratase-deficiency - Genetics
  2. Megalencephalic leukoencephalopathy with subcortical cysts 
    ... people also have leukoencephalopathy, an abnormality of the brain's white ... away (atrophy). Individuals affected with this condition may develop cysts ...
    https://medlineplus.gov/...eukoencephalopathy-with-subcortical-cysts - Genetics
  3. Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart 
    ... the brain (the corpus callosum), a tissue called white matter, the fluid-filled ... or breakdown (atrophy) of the nerves that carry information from the ...
    https://medlineplus.gov/...thout-anomalies-of-the-brain-eye-or-heart - Genetics
  4. TUBB4A-related leukodystrophy 
    ... the brain, particularly in the putamen, cerebellum, and white matter. During brain development, microtubules help move nerve cells (neurons) to ... the brain, particularly in the putamen, cerebellum, and white matter. ... these brain regions underlie the movement, speech, and learning problems ...
    https://medlineplus.gov/.../condition/tubb4a-related-leukodystrophy - Genetics
  5. Hypomyelination and congenital cataract 
    ... disorders called leukoencephalopathies. Leukoencephalopathies involve abnormalities of the brain's white matter. White matter consists of nerve fibers covered by ...
    https://medlineplus.gov/.../hypomyelination-and-congenital-cataract - Genetics
  6. CLCN2-related leukoencephalopathy 
    ... this condition have leukoencephalopathy, an abnormality of the brain's white matter that can be detected with medical imaging. White ...
    https://medlineplus.gov/.../clcn2-related-leukoencephalopathy - Genetics
  7. Peroxisomal acyl-CoA oxidase deficiency 
    ... leads to a loss of myelin-containing tissue (white matter) in the brain and spinal cord; loss of white matter is described as leukodystrophy. Leukodystrophy is likely involved ...
    https://medlineplus.gov/.../peroxisomal-acyl-coa-oxidase-deficiency - Genetics
  8. Fatty acid hydroxylase-associated neurodegeneration 
    ... transmission of nerve impulses. The part of the brain and spinal cord that contains myelin is called white matter.The FA2H gene mutations that cause FAHN reduce ...
    https://medlineplus.gov/...-hydroxylase-associated-neurodegeneration - Genetics
  9. Pelizaeus-Merzbacher-like disease type 1 
    ... type 1 is an inherited condition involving the brain and spinal cord (central nervous system). This disease is one of a group of genetic disorders called leukodystrophies. Leukodystrophies are abnormalities of the nervous system's white matter, which consists of nerve fibers covered by a ...
    https://medlineplus.gov/.../pelizaeus-merzbacher-like-disease-type-1 - Genetics
  10. Pelizaeus-Merzbacher disease 
    ... Merzbacher disease is an inherited condition involving the brain and ... nervous system's white matter, which consists of nerve fibers covered by a ...
    https://medlineplus.gov/.../condition/pelizaeus-merzbacher-disease - Genetics
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