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What is Congenital disorder of glycosylation type 1I?

What is Congenital disorder of glycosylation type 1I?

  • Congenital disorder of glycosylation type 1I: 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 Ii is caused by a defect on chromosome 9q22 and involves a defect on the ALG2 gene.

Congenital disorder of glycosylation type 1I: Introduction

Types of Congenital disorder of glycosylation type 1I:

Broader types of Congenital disorder of glycosylation type 1I:

What causes Congenital disorder of glycosylation type 1I?

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

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

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

Congenital disorder of glycosylation type 1I: Testing

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

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

How is it treated?

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

Name and Aliases of Congenital disorder of glycosylation type 1I

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

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

CDG Ii, CDG1i, CDG syndrome type Ii

 

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