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Congenital disorder of glycosylation type 1H

Congenital disorder of glycosylation type 1H: Introduction

Congenital disorder of glycosylation type 1H: Congenital disorders of glycosylation is a group of very rare inherited metabolic disorder where defective carbohydrate compounds are attached to glycoproteins and thus impairing glycoprotein function. Type Ih is caused by a defect on chromosome 11pter-p15.5 and involves the gene for a particular enzyme (dolichyl-P-glucose:Glc-1-Man-9-GlcNAc-2-PP-dolichyl-alpha-3-glucosyltransferase). More detailed information about the symptoms, causes, and treatments of Congenital disorder of glycosylation type 1H is available below.

Symptoms of Congenital disorder of glycosylation type 1H

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Causes of Congenital disorder of glycosylation type 1H

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Congenital disorder of glycosylation type 1H: Undiagnosed Conditions

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Misdiagnosis and Congenital disorder of glycosylation type 1H

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More information about Congenital disorder of glycosylation type 1H

  1. Congenital disorder of glycosylation type 1H: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
 

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