dictionary help| gangliosidosis g(m1) | medical dictionary |
Form of gangliosidosis characterised by accumulation of g(m1) ganglioside and oligosaccharides, and caused by an absence or severe deficiency of beta-galactosidase a. The three phenotypes of g(m1) gangliosidosis are called infantile (generalised), juvenile, and adult (types 1, 2, and 3 respectively), referring to the age at which clinical manifestations appear.
(12 Dec 1998)
ganglioside O-acetyltransferase, gangliosidoses, gangliosidosis < Prev | Next > gangosa, gangrene, gangrenous
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