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Glycogen Storage Disease Type VIII

An x-linked recessive hepatic glycogen storage disease resulting from lack of expression of phosphorylase-b-kinase activity. Symptoms are relatively mild; hepatomegaly, increased liver glycogen, and decreased leukocyte phosphorylase are present. Liver shrinkage occurs in response to glucagon.
Also Known As:
Glycogenosis 8
Networked: 1 relevant articles (0 outcomes, 0 trials/studies)

Disease Context: Research Results

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Glycogen Storage Disease Type VIII:
1. GlycogenIBA