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Congenital disorder of glycosylation type 1C

Congenital disorder of glycosylation type 1C: Introduction

Congenital disorder of glycosylation type 1C: A very rare inherited metabolic disorder where defective carbohydrate compounds are attached to glycoproteins and thus impairing glycoprotein function. Type 1C has a ?1,3-glucosyl-transferase enzyme defect. More detailed information about the symptoms, causes, and treatments of Congenital disorder of glycosylation type 1C is available below.

Symptoms of Congenital disorder of glycosylation type 1C

See full list of 13 symptoms of Congenital disorder of glycosylation type 1C

Wrongly Diagnosed with Congenital disorder of glycosylation type 1C?

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Disease Topics Related To Congenital disorder of glycosylation type 1C

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Medical Textbooks Online about Congenital disorder of glycosylation type 1C

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Book excerpts: Copyright © 2008 Lippincott Williams & Wilkins. All rights reserved.

Less Common Symptoms of Congenital disorder of glycosylation type 1C

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Congenital disorder of glycosylation type 1C: Undiagnosed Conditions

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Misdiagnosis and Congenital disorder of glycosylation type 1C

Mild worm infections undiagnosed in children: Human worm infestations, esp. threadworm, can be overlooked in some cases, because it may cause only mild or even absent symptoms. Although...read more »

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