A glycogen storage disease (GSD, also glycogenosis and dextrinosis) is a metabolic disorder caused by a deficiency of an enzyme or transport protein affecting...
68 KB (6,172 words) - 04:04, 10 October 2024
Glycogen storage disease type II (GSD-II), also called Pompe disease, and formerly known as GSD-IIa or Limb–girdle muscular dystrophy2V, is an autosomal...
36 KB (4,291 words) - 16:08, 11 October 2024
Glycogen storage disease type I (GSD I) is an inherited disease that prevents the liver from properly breaking down stored glycogen, which is necessary...
45 KB (5,801 words) - 16:07, 11 October 2024
Glycogen storage disease type V (GSD5, GSD-V), also known as McArdle's disease, is a metabolic disorder, one of the metabolic myopathies, more specifically...
58 KB (6,658 words) - 16:32, 11 October 2024
Glycogen storage disease type IV (GSD IV), or Andersen's Disease, is a form of glycogen storage disease, which is caused by an inborn error of metabolism...
8 KB (891 words) - 04:01, 5 February 2023
Glycogen storage disease type III (GSD III) is an autosomal recessive metabolic disorder and inborn error of metabolism (specifically of carbohydrates)...
11 KB (997 words) - 15:09, 29 July 2024
Glycogen storage disease type VI (GSD VI) is a type of glycogen storage disease caused by a deficiency in liver glycogen phosphorylase or other components...
4 KB (295 words) - 02:04, 27 January 2021
Danon disease (or glycogen storage disease Type IIb) is a metabolic disorder. Danon disease is an X-linked lysosomal and glycogen storage disorder associated...
10 KB (1,111 words) - 20:25, 24 January 2024
media related to Glycogen phosphorylase. GeneReviews/NCBI/NIH/UW entry on Glycogen Storage Disease Type VI - Hers disease Glycogen+phosphorylase at the...
26 KB (2,918 words) - 16:51, 15 September 2024
Glycogen storage disease type 0 is a disease characterized by a deficiency in the glycogen synthase enzyme (GSY). Although glycogen synthase deficiency...
12 KB (1,383 words) - 12:21, 20 September 2022