GM1 gangliosidosis type 1

GM1 gangliosidosis type 1 is the severe infantile form of GM1 gangliosidosis with variable neurological and systemic manifestations.

Also known as: Norman-Landing disease, infantile GM1 gangliosidosis, Beta galactosidase deficiency type 1, Beta-galactosidase-1 deficiency, GLB deficiency type 1, GM1-gangliosidosis, type 1, GM1-gangliosidosis, type I, GM1-gangliosidosis, type I, with Cardiac involvement

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