Hereditary CNS demyelinating disease
| Hereditary CNS demyelinating disease | |
|---|---|
| Specialty | Neurology, medical genetics, endocrinology  |
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[verification needed]
- Canavan disease[verification needed]
- Krabbe disease[verification needed]
- leukoencephalopathy with vanishing white matter[verification needed]
- megalencephalic leukoencephalopathy with subcortical cysts[verification needed]
- metachromatic leukodystrophy[verification needed]
- X-linked adrenoleukodystrophy[verification needed]
References
- ^ "Hereditary Central Nervous System Demyelinating Diseases - Genetics Home Reference". Archived from the original on 2010-04-08. Retrieved 2009-03-11.
External links
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