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Glycogen storage disease type 1C

Glycogen storage disease type 1C: Introduction

Glycogen storage disease type 1C: A genetic metabolic disorder involving a deficiency of the enzyme glucose-6-phosphatase (due to a defect in the microsomal phosphate) which results in the accumulation of glycogen in various tissues. G6P is stored as glycogen until the body needs to convert it to a sugar for energy. The enzyme deficiency prevents the conversion and hence low blood sugar levels result. More detailed information about the symptoms, causes, and treatments of Glycogen storage disease type 1C is available below.

Symptoms of Glycogen storage disease type 1C

Home Diagnostic Testing

Home medical testing related to Glycogen storage disease type 1C:

Wrongly Diagnosed with Glycogen storage disease type 1C?

Causes of Glycogen storage disease type 1C

Read more about causes of Glycogen storage disease type 1C.

Disease Topics Related To Glycogen storage disease type 1C

Research the causes of these diseases that are similar to, or related to, Glycogen storage disease type 1C:

Misdiagnosis and Glycogen storage disease type 1C

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 are...read more »

Glycogen storage disease type 1C: Research Doctors & Specialists

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Glycogen storage disease type 1C: Animations

Glycogen storage disease type 1C: Broader Related Topics

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More information about Glycogen storage disease type 1C

  1. Glycogen storage disease type 1C: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
 

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