GM1 gangliosidosis type 2

GM1 gangliosidosis type 2 is a clinically variable, infancy or childhood-onset form of GM1 gangliosidosis characterized by normal early development and psychomotor regression between seven months and three years of age.

Also known as: juvenile GM1 gangliosidosis, late-infantile GM1 gangliosidosis, GM1-gangliosidosis, type 2, GM1-gangliosidosis, type II, gangliosidosis generalised GM1 juvenile type, gangliosidosis generalised GM1 type 2, gangliosidosis generalized GM1 juvenile type, gangliosidosis generalized GM1 type 2

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