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What is Congenital disorder of glycosylation type 1G?

What is Congenital disorder of glycosylation type 1G?

  • Congenital disorder of glycosylation type 1G: 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 IG is caused by a defect on chromosome 22q13.33 and involves the gene for a particular enzyme (dolichyl-P-mannose:Man-7-GlcNAc-2-PP-dolichyl-alpha-6-mannosyltransferase).

Congenital disorder of glycosylation type 1G: Introduction

Types of Congenital disorder of glycosylation type 1G:

Broader types of Congenital disorder of glycosylation type 1G:

What causes Congenital disorder of glycosylation type 1G?

Causes of Congenital disorder of glycosylation type 1G: see causes of Congenital disorder of glycosylation type 1G

What are the symptoms of Congenital disorder of glycosylation type 1G?

Symptoms of Congenital disorder of glycosylation type 1G: see symptoms of Congenital disorder of glycosylation type 1G

Congenital disorder of glycosylation type 1G: Testing

Diagnostic testing: see tests for Congenital disorder of glycosylation type 1G.

Misdiagnosis: see misdiagnosis and Congenital disorder of glycosylation type 1G.

How is it treated?

Doctors and Medical Specialists for Congenital disorder of glycosylation type 1G: Medical Geneticist ; see also doctors and medical specialists for Congenital disorder of glycosylation type 1G.
Treatments for Congenital disorder of glycosylation type 1G: see treatments for Congenital disorder of glycosylation type 1G

Name and Aliases of Congenital disorder of glycosylation type 1G

Main name of condition: Congenital disorder of glycosylation type 1G

Other names or spellings for Congenital disorder of glycosylation type 1G:

CDG Ig, CDG1g, CDG syndrome type Ig

 

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