GM1 gangliosidosis is a rare genetic lysosomal storage disease caused by a deficiency of the beta-galactosidase enzyme. This enzyme is responsible for breaking down a fatty substance called GM1 ganglioside within cells. A deficiency of this enzyme causes GM1 gangliosides to accumulate in tissues throughout the body, especially in the brain and central nervous system. There are three m... https://prachicmi.livepositively.com/gm1-gangliosidosis-causes-treatment-options-and-management/new=1