GM2-gangliosidosis, AB variant is a rare, autosomal recessive metabolic disorder that causes progressive destruction of nerve cells in the brain and spinal...
8 KB (914 words) - 14:25, 12 October 2024
Sandhoff disease (redirect from B variant of the Hexosaminidase GM2 gangliosidosis)
GM1-gangliosidosis in 1963, Sandhoff disease in 1968, Tay-Sachs-Disease, the AB-variant of GM2-Gangliosidosis and the B1-variant of GM2-gangliosidosis. The...
24 KB (3,024 words) - 14:53, 23 October 2024
infantile Sandhoff disease, is usually fatal by early childhood. GM2-gangliosidosis, AB variant is a rare, autosomal recessive metabolic disorder that causes...
12 KB (1,214 words) - 14:23, 12 October 2024
GM2A (redirect from Ganglioside GM2 activator protein)
in an autosomal recessive pattern, result in GM2-gangliosidosis, AB variant, a rare GM2 gangliosidosis that has symptoms and pathology identical with...
10 KB (1,315 words) - 08:31, 18 August 2023
(alpha-galactosidase B) Beta-galactosidase / GM1 gangliosidosis Infantile Juvenile Adult / chronic GM2 gangliosidosis AB variant Activator deficiency Sandhoff disease...
18 KB (1,831 words) - 14:49, 30 October 2024
Tay–Sachs disease (redirect from GM2-gangliosidosis, B, B1, AB variant)
researchers had identified three variant forms of GM2 gangliosidosis, including Sandhoff disease and the AB variant of GM2-gangliosidosis, accounting for false negatives...
58 KB (6,401 words) - 02:47, 22 September 2024
failure on a metabolic pathway. For example, Tay–Sachs disease, GM2-gangliosidosis, AB variant, and Sandhoff disease might easily have been defined together...
10 KB (1,252 words) - 19:17, 28 October 2024
Gangliosides: Gangliosidosis GM1 gangliosidoses GM2 gangliosidoses Tay–Sachs disease Sandhoff disease GM2-gangliosidosis, AB variant Glycolipids Fabry's...
10 KB (652 words) - 23:45, 13 August 2024
GM 2 gangliosidosis refers to several similar genetic disorders: Tay–Sachs disease Sandhoff disease GM2-gangliosidosis, AB variant This set index article...
469 bytes (58 words) - 03:58, 28 August 2023
corneal dystrophy type I Granular corneal dystrophy type II GM2-gangliosidosis, AB variant Homocystinuria 3-Methylcrotonyl-CoA carboxylase deficiency Myelodysplastic...
32 KB (2,298 words) - 22:55, 28 March 2024
type VIII Glycogenosis, type 0 Glycosuria GM2 gangliosidosis, 0 variant GM2-gangliosidosis, B, B1, AB variant GMS syndrome Goitre Goldberg–Bull syndrome...
10 KB (846 words) - 12:38, 3 March 2024
GM1-gangliosidosis, type I; 230500; GLB1 GM1-gangliosidosis, type II; 230600; GLB1 GM1-gangliosidosis, type III; 230650; GLB1 GM2-gangliosidosis, AB variant;...
234 KB (18,877 words) - 15:43, 9 May 2024
100.435.825.300.300.920 – Tay–Sachs disease, AB variant MeSH C18.452.100.100.435.825.300.400 – gangliosidosis gm1 MeSH C18.452.100.100.435.825.400 – Gaucher...
47 KB (4,274 words) - 16:49, 9 February 2024
1970s, researchers had identified three variant forms of GM2 gangliosidosis, including Sandhoff disease and AB variant, accounting for false negatives in carrier...
14 KB (1,811 words) - 23:15, 24 February 2024
150.435.825.300.300.920 – Tay–Sachs disease, AB variant MeSH C16.320.565.150.435.825.300.400 – gangliosidosis GM1 MeSH C16.320.565.150.435.825.400 – Gaucher...
78 KB (6,496 words) - 05:23, 12 April 2022
435.825.300.300.750 – tay-sachs disease, ab variant MeSH C10.228.140.163.100.435.825.300.400 – gangliosidosis gm1 MeSH C10.228.140.163.100.435.825.300...
109 KB (9,229 words) - 16:51, 9 February 2024