What is another word for Tay Sachs Disease Ganglioside?
Pronunciation: [tˈe͡ɪ sˈaks dɪzˈiːz ɡˈaŋɡlɪˌɒsa͡ɪd] (IPA) 
Tay Sachs Disease Ganglioside is a rare genetic disorder that primarily affects the nervous system. It is characterized by the accumulation of a specific type of lipid called ganglioside GM2 in the brain and spinal cord. Synonyms for this debilitating disease include GM2 gangliosidoses, Hexosaminidase A deficiency, and Tay Sachs disease. GM2 gangliosidoses encompasses a group of disorders caused by mutations in the HEXA gene, resulting in the absence or impaired activity of the Hexosaminidase A enzyme. These synonyms highlight the underlying genetic and biochemical processes involved in the disease, emphasizing the need for further research and therapeutic interventions to alleviate the suffering associated with Tay Sachs Disease Ganglioside.
