Definition of Gangliosidoses. Meaning of Gangliosidoses. Synonyms of Gangliosidoses

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Definition of Gangliosidoses

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Meaning of Gangliosidoses from wikipedia

- autosomal recessive and affect males and females equally. GM1 gangliosidoses - GM1 GM2 gangliosidoses - GM2 Sphingolipidoses#Overview Prayson, Richard A. (2012)...
- 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 GM1 gangliosidoses, usually shortened to GM1, are gangliosidoses caused by mutation in the GLB1 gene resulting in a deficiency of beta-galactosidase...
- disorders Gangliosidoses (including Tay–Sachs disease (E75.0-E75.1) - they are a subtype of sphingolipidoses Sphingolipidoses that are not gangliosidoses, including...
- Mahuran DJ (1999). "Biochemical consequences of mutations causing the GM2 gangliosidoses". Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease....
- juvenile- or adult-onset forms. Gangliosides: Gangliosidosis GM1 gangliosidoses GM2 gangliosidoses Tay–Sachs disease Sandhoff disease GM2-gangliosidosis, AB...
- second monosialic ganglioside discovered. It is ****ociated with GM2 gangliosidoses such as Tay–Sachs disease. Ganglioside GM2 activator protein Sphingolipidoses...
- needed] GM1 storage disease, one of a family of conditions called GM1 gangliosidoses, is a recessive, genetic disorder that is inevitably fatal. It is caused...
- of the sphingolipidoses may be classified into either GM1 gangliosidoses or GM2 gangliosidoses. Tay–Sachs disease belongs to the latter. Other lipid storage...
- name. N-Acetyl-L-Leucine is being studied for the treatment of GM2 gangliosidoses (Tay-Sachs and Sandhoff diseases) and ataxia-telangiectasia. "Aqneursa-...