The GM2 gangliosidoses are a group of three related genetic disorders that result from a deficiency of the enzyme beta-hexosaminidase. This enzyme catalyzes the ...
Background The GM2 gangliosidoses are a group of lysosomal lipid storage disorders caused by mutations in at least 1 of 3 recessive genes: HEXA, HEXB, and ...
GM2-gangliosidosis, AB variant is a rare, autosomal recessive metabolic disorder that causes progressive destruction of nerve cells in the brain and spinal cord.
The GM2 gangliosidoses are a group of related genetic disorders that result from a deficiency of the enzyme beta-hexosaminidase. This enzyme catalyzes the ...
The GM1 gangliosidoses are caused by a deficiency of beta-galactosidase, ... GM1 gangliosidoses; GM2 gangliosidoses; Lipid storage disorders;
The GM2-gangliosidoses are a group of disorders caused by excessive accumulation of ganglioside ... GM2-gangliosidosis AB variant is characterized by normal ...
Click to launch & play an online audio visual presentation by Prof. Don Mahuran on GM2 Gangliosidoses, part of a collection of online lectures.
Gangliosidosis is an autosomal-recessive genetic lysosomal storage disease of dogs characterized by various neurological symptoms. This disease, which mirrors that of ...
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Gangliosidoses information page compiled by the National Institute of Neurological ... The GM2 gangliosidoses include Tay-Sachs disease and its more ...