Overview

Hers' disease


Show Summary Details

Quick Reference

An autosomal recessive glycogen storage disease (glycogen storage disease VI) in which there is a deficiency of liver phosphorylase (EC 2.4.1.1). Affected individuals show mild to moderate hypoglycaemia, mild ketosis, growth retardation, and prominent hepatomegaly.

Subjects: Medicine and Health.


Reference entries

Users without a subscription are not able to see the full content. Please, subscribe or login to access all content.