Sphingolipidoses are a class of lipid storage disorders relating to sphingolipid metabolism. The main members of this group are Niemann-Pick disease, Fabry disease, Krabbe disease, Gaucher disease, Tay-Sachs disease and Metachromatic leukodystrophy. They are generally inherited in an autosomal recessive fashion, but notably Fabry disease is X-link...
Found on
http://en.wikipedia.org/wiki/Sphingolipidoses
Lysosomal storage diseases characterised by failure to degrade sphingolipids and resulting in their abnormal storage. ... (12 Dec 1998) ...
Found on
http://www.encyclo.co.uk/local/20973
No exact match found.
