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leukodystrophy

see NINDS Leukodystrophy Information Page

Specific

adrenoleukodystrophy Alexander's leukodystrophy (Alexander disease) autosomal dominant adult-onset leukodystrophy (autosomal dominant Pelizaeus-Merzbacher disease) globoid leukodystrophy; Krabbe's leukodystrophy; galactosylceramide beta-galactosidase deficiency; galactosylceramidase deficiency leukodystrophy hypomyelinating type-4; mitochondrial HSP60 chaperonopathy; mitCHAP-60 disease metachromatic leukodystrophy Pelizaeus-Merzbacher disease Refsum disease; phytanic acid oxidase deficiency; phytanic acid storage disease spongiform leukodystrophy; Canavan's disease; Canavan-van Bogaert-Bertrand spongy degeneration Zellweger syndrome; cerebrohepatorenal syndrome

General

genetic disease of the central nervous system

References

  1. National Institute of Neurological Disorders and Stroke (NINDS) NINDS Leukodystrophy Information Page https://www.ninds.nih.gov/disorders/all-disorders/leukodystrophy-information-page