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russo
гликогеноз
português
glicogenose
espanhol
enfermedad por almacenamiento de glucógeno
catalão
glicogenosi
Wikidata

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.

glicogenose
1
A 17-yr-old female received a liver transplant for type I glycogen storage disease.
Pubmed
2
The recipient was a 2-year-old girl affected by glycogen storage disease type IV.
Pubmed
3
A boy with marked hepatomegaly and motor weakness was investigated for glycogen storage disease.
Pubmed
4
Patients with glycogen storage disease (GSD) type IA were not excluded.
Pubmed
5
Any lesions that were suspected of neurogenic atrophy, traumatic muscular degeneration, glycogen storage disease or other porcine muscular disorders were not observed.
Pubmed
6
Glycogen storage disease type IX (GSD type IX) results from a deficiency of hepatic phosphorylase kinase activity.
Pubmed
7
Glycogen storage diseases (GSD) are inherited metabolic disorders of glycogen metabolism due to intracellular enzyme deficiency resulting in abnormal storage of glycogen in tissues.
Pubmed