Glycogen Storage Disease Type VIII
| Definition: |
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. |
| Notes: |
do not use /congen & do not coord with INFANT, NEWBORN, DISEASES |
| Previously Indexed: |
Glycogenosis (1966-1974) |
Glycogen Storage Disease Type VIII Definitions and Terms
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