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Glycogen storage disease type 1D

Glycogen storage disease type 1D: Introduction

Glycogen storage disease type 1D: A genetic metabolic disorder involving a deficiency of the enzyme glucose-6-phosphatase (due to a defect in the microsomal glucose transporter) 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 1D is available below.

Symptoms of Glycogen storage disease type 1D

Home Diagnostic Testing

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Wrongly Diagnosed with Glycogen storage disease type 1D?

Glycogen storage disease type 1D: Related Patient Stories

Causes of Glycogen storage disease type 1D

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

Disease Topics Related To Glycogen storage disease type 1D

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Misdiagnosis and Glycogen storage disease type 1D

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Glycogen storage disease type 1D: Research Doctors & Specialists

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Glycogen storage disease type 1D: Animations

Glycogen storage disease type 1D: Broader Related Topics

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