Global GM2 Gangliosidosis Market | PMI

Health

Source: Global GM2 Gangliosidosis Market | PMI

GM2 Gangliosidosis, often known as Tay-Sachs disease, is caused by a mutation in the HEXA genes, which results in muscular atrophy. Because this disease has no known cure, therapy is mainly symptom-based. Some of the signs and symptoms include exaggerated reactions to loud noises, seizures, loss of movement, vision, and hearing, mucus collection in the lungs, and other symptoms.

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