| lipidoses | Storage diseases in which the missing enzyme is one that degrades sphingolipids sphingomyelin, ceramides, gangliosides). In Tay Sachs disease the lesion is in hexosiminidase A, an enzyme that degrades ganglioside Gm2, in Gaucher's disease, glucocerebrosidase, in Niemann-Pick disease, sphingomyelinase. (18 Nov 1997) |
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