A RARE CAUSE OF BOTH HYPO AND HYPERGLYCEMIA; GLYCOGEN STORAGE DISEASE TYPE 0: A CASE REPORT

A RARE CAUSE OF BOTH HYPO AND HYPERGLYCEMIA; GLYCOGEN STORAGE DISEASE TYPE 0: A CASE REPORT

Glycogen-storage disease type 0A is a rare autosomal recessively inherited disease resulting from a hepatic glycogen synthase enzyme deficiency. Glycogen-storage disease type 0A is characterized by fasting ketotic hypoglycaemia, postprandial hyperglycemia and lactic acidemia without hepatomegaly. In...

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Bibliographic Details
Main Authors: Meryem Karaca, Halil Aslan
Format: Article
Language:English
Published: Istanbul University Press 2021-07-01
Series:İstanbul Tıp Fakültesi Dergisi
Subjects:
glycogen storage disease type 0a
ketotic hypoglycaemia
hyperglycaemia
lactic acidemia
Online Access:https://cdn.istanbul.edu.tr/file/JTA6CLJ8T5/6A32CE37D6D84CA08F7E773AAFD36749
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