Hereditary CNS demyelinating disease

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Hereditary CNS demyelinating disease
Classification and external resources
ICD-9 330.0
MeSH D020279

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.)

Examples include:[1]

References[edit]