GM1 gangliosidosis

A rare lysosomal storage disorder characterized biochemically by deficient beta-galactosidase activity and clinically by a wide range of variable neurovisceral, ophthalmological and dysmorphic features.

Also known as: Beta-galactosidase-1 deficiency, GLB1 deficiency, GM>1< gangliosidosis, Landing disease, Landing syndrome, gangliosidosis GM1, Beta galactosidase 1 deficiency, Beta-galactosidosis

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