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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

Home Diagnostic Testing

Home medical testing related to Glycogen storage disease type 6:

Wrongly Diagnosed with Glycogen storage disease type 6?

Glycogen storage disease type 6: Related Patient Stories

Glycogen storage disease type 6: Complications

Read more about complications of Glycogen storage disease type 6.

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 reasons...read more »

Glycogen storage disease type 6: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Glycogen storage disease type 6: Animations

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

Glycogen storage disease type 6: Broader Related Topics

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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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