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Results 1 - 4 of 4 for GM2 gangliosidosis
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  1. GM2 activator deficiency 
    GM2 activator deficiency (sometimes called GM2 gangliosidosis, AB variant) is a rare inherited disorder that causes progressive brain injury. Most individuals with GM2 activator deficiency have the acute ...
    https://medlineplus.gov/genetics/condition/gm2-activator-deficiency - Genetics
  2. Tay-Sachs disease 
    ... to as a lysosomal storage disorder or a GM2-gangliosidosis. HEXA This condition is inherited in an autosomal ... signs and symptoms of the condition. B variant GM2 gangliosidosis GM2 gangliosidosis, type 1 HexA deficiency Hexosaminidase A ...
    https://medlineplus.gov/genetics/condition/tay-sachs-disease - Genetics
  3. Sandhoff disease 
    ... to as a lysosomal storage disorder or a GM2-gangliosidosis. Sandhoff disease is one of three conditions caused ... two conditions are called Tay-Sachs disease and GM2-gangliosidosis, AB variant, which are caused by variants in ...
    https://medlineplus.gov/genetics/condition/sandhoff-disease - Genetics
  4. GM1 gangliosidosis 
    ... D'Azzo A, Tifft CJ. The GM1 and GM2 Gangliosidoses: Natural History and Progress toward Therapy. Pediatr Endocrinol ...
    https://medlineplus.gov/genetics/condition/gm1-gangliosidosis - Genetics