Tay-Sachs disease AB variant

GM2 gangliosidosis, AB variant is an extremely rare, severe genetic disorder characterized by progressive neurological decline due to ganglioside activator deficiency.

Also known as: hexosaminidase activator deficiency, Ab variant GM2-gangliosidosis, GM2 activator deficiency, GM2 gangliosidosis, AB variant, GM2-gangliosidosis, AB variant, Tay-Sachs disease, AB variant

0 clinical trials for this condition and its sub-types.