Gangliosidosis
An autosomal recessive lysosomal storage disease characterized by deficiency of the enzyme acid beta-galactosidase, resulting in the accumulation of acid lipids in the nervous system. Signs and symptoms include neurologic disturbances, muscle atrophy, dystonia, eye abnormalities, and formation of angiokeratomas.
Disease Alternative Name
Top Gangliosidosis Doctors on Curofy
Top doctors who continously share their opinions on GangliosidosisBHASKARA HOSPITAL
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