Glycogen metabolism disorder that has material basis in enzymes deficiencies necessary in the processing of glycogen synthesis or breakdown within muscles, liver, and other cell types.
Mutation within these genes has been shown to result in GSD type IX.
2
Four children with GSD I were studied over a 72-h period.
3
The Company invests in these sectors through its subsidiaries, forming the GSD Group.
4
The GSD has a large and committed flock, and we sometimes make .
5
Objective: Analysis of epidemiological data concerning GSD I in Tunisia.
1
A subdivision of glycogenosis type IV in four subtypes is proposed, based on age of onset.
2
Three related patients are described with glycogenosis type IV with an unusual clinical presentation resulting in perinatal death.
Ús de glycogen storage disease en anglès
1
A 17-yr-old female received a liver transplant for type I glycogenstoragedisease.
2
The recipient was a 2-year-old girl affected by glycogenstoragedisease type IV.
3
A boy with marked hepatomegaly and motor weakness was investigated for glycogenstoragedisease.
4
Patients with glycogenstoragedisease (GSD) type IA were not excluded.
5
Any lesions that were suspected of neurogenic atrophy, traumatic muscular degeneration, glycogenstoragedisease or other porcine muscular disorders were not observed.
6
Glycogenstoragedisease type IX (GSD type IX) results from a deficiency of hepatic phosphorylase kinase activity.
7
Glycogenstoragediseases (GSD) are inherited metabolic disorders of glycogen metabolism due to intracellular enzyme deficiency resulting in abnormal storage of glycogen in tissues.