Glycogen storage disease type 6
Glycogen storage disease type 6: Introduction
Glycogen storage disease type 6: A rare, generally mild form of inherited glycogen storage disease where a deficiency of phosphorylase b kinase leads to hypoglycemia and accumulation of glycogen in the liver.
More detailed information about the symptoms,
causes, and treatments of Glycogen storage disease type 6 is available below.
Symptoms of Glycogen storage disease type 6
See full list of 9
symptoms of Glycogen storage disease type 6
Home Diagnostic Testing
Home medical testing related to Glycogen storage disease type 6:
- Liver Health & Hepatitis: Home Testing
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Wrongly Diagnosed with Glycogen storage disease type 6?
Glycogen storage disease type 6: Related Patient Stories
Glycogen storage disease type 6: Complications
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Causes of Glycogen storage disease type 6
Read more about causes of Glycogen storage disease type 6.
Disease Topics Related To Glycogen storage disease type 6
Research the causes of these diseases that are similar to, or related to, Glycogen storage disease type 6:
Misdiagnosis and Glycogen storage disease type 6
Chronic liver disease often undiagnosed: One study reported that 50% of patients
with a chronic liver disease remain undiagnosed by their primary physician.
The...read more »
Read more about Misdiagnosis and Glycogen storage disease type 6
Glycogen storage disease type 6: Research Doctors & Specialists
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Glycogen storage disease type 6: Animations
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Prognosis for Glycogen storage disease type 6
Prognosis for Glycogen storage disease type 6:
often symptoms are so mild that they're not noticed until adulthood
More about prognosis of Glycogen storage disease type 6
Glycogen storage disease type 6: Broader Related Topics
Types of Glycogen storage disease type 6
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Definitions of Glycogen storage disease type 6:
A hepatic GLYCOGEN STORAGE DISEASE in which there is an apparent deficiency of hepatic phosphorylase (GLYCOGEN PHOSPHORYLASE, LIVER FORM) activity.
- (Source - Diseases Database)
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