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Hereditary CNS demyelinating disease information


Hereditary CNS demyelinating disease
SpecialtyNeurology, medical genetics, endocrinology Edit this on Wikidata

A hereditary CNS demyelinating disease is a demyelinating central nervous system disease that is primarily due to an inherited genetic condition. (This is in contrast to autoimmune demyelinating conditions, such as multiple sclerosis, or conditions such as central pontine myelinolysis that are associated with acute acquired insult.)[citation needed]

Examples include:[1]

  • Alexander disease
  • Canavan disease
  • Krabbe disease
  • leukoencephalopathy with vanishing white matter
  • megalencephalic leukoencephalopathy with subcortical cysts
  • metachromatic leukodystrophy
  • X-linked adrenoleukodystrophy
  1. ^ "Hereditary Central Nervous System Demyelinating Diseases - Genetics Home Reference". Archived from the original on 2010-04-08. Retrieved 2009-03-11.

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Hereditary CNS demyelinating disease

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neuropathy, demyelinating disease, multiple sclerosis, Friedreich’s ataxia, vitamin B12 deficiency, neurosyphilis, migraine, ischemic disease, tumor compressing...

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Stephen Waxman

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