GM2 gangliosidosis, HEXB-related dog
MONDO:1010883A lysosomal storage disease in dogs due to a mutation in the HEXB gene. There is a buildup of GM2 gangliosides in tissues due to the lack of the enzyme hexosaminidase. Characterised by progressive neuromuscular dysfunction and impaired growth from an early age.
Also known as: gangliosidosis, GM2, type II (Sandhoff or variant 0), dog
0 clinical trials for this condition and its sub-types, 0 tagged with GM2 gangliosidosis, HEXB-related dog itself.
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