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"tay-sachs"
- Tay-Sachs disease is a rare, inherited disorder that is characterized by neurological problems caused by the death ... central nervous system).The most common form of Tay-Sachs disease, known as infantile Tay-Sachs disease, becomes ...
- ... condition. GM2 gangliosidosis, AB variant Hexosaminidase activator deficiency Tay-Sachs disease, AB variant Genetic Testing Registry: Tay-Sachs disease, variant AB GM2-gangliosidosis, B, B1, AB ...
- ... GM2 ganglioside. The other two conditions are called Tay-Sachs disease and GM2-gangliosidosis, AB variant, which are ... on burden of disease manifestations in late-onset Tay-Sachs and Sandhoff diseases. Orphanet J Rare Dis. 2020 ...