Gangliosidoses GM2

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Gangliosidoses GM2

Inherited diseases characterized by the accumulation of G(M2) GANGLIOSIDE in central nervous system lysosomes and variably in other tissues. Subtypes include the BETA-N-ACETYLHEXOSAMINIDASE deficiency variants TAY-SACHS DISEASE and SANDHOFF DISEASE, as well as the TAY-SACHS DISEASE, AB VARIANT and an adult onset form of GM2 Gangliosidosis.