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Hereditary CNS demyelinating disease: Wikis

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Updated live from Wikipedia, last check: June 02, 2012 02:41 UTC (44 seconds ago)

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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

  1. ^ "Hereditary Central Nervous System Demyelinating Diseases - Genetics Home Reference". http://ghr.nlm.nih.gov/conditionGroup=hereditarycentralnervoussystemdemyelinatingdiseases. Retrieved 2009-03-11.  
(LSD) Inborn error of lipid metabolism: lipid storage disorders (E75, 272.7-272.8)
Sphingolipidoses
(to ceramide)
NCL
Other
see also enzymes, sphingolipids
Pathology of the nervous system, primarily CNS (G04–G47, 323–349)
Inflammation
Both/either
Brain/
encephalopathy
Episodic/
paroxysmal
Other
Spinal cord/
myelopathy
Both/either
central nervous system navs: anat/physio/dev, noncongen/congen/neoplasia, symptoms+signs/eponymous, proc







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