Type 3 (adult) GM1 gangliosidosis (medical condition)

A rare biochemical disorder involving a deficiency of an enzyme (beta-galactosidase A) which results in the accumulation of harmful chemicals (GM1 gangliosides) in the central nervous system and other body tissues. Type III involves a lesser degree of accumulation than type II or I. See also Gangliosidosis GM1 type 3

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