Definition
Glycogen storage disease type III is a metabolic disease characterized by debranching enzyme deficiency, hepatomegaly, and myopathy.
Symptoms
- Hepatomegaly
- Hypoglycemia
- Myopathy
- Growth retardation
Reasons
AGL gene mutation.
Diagnosis
Liver biopsy, genetic testing.
Treatment
High protein diet.
Which Polyclinic Should You Apply To?
Metabolism Polyclinic
What to Do in an Emergency?
In case of hypoglycemia, emergency services should be consulted.
This page is for general information purposes only.