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What is Congenital disorder of glycosylation type 1F?

What is Congenital disorder of glycosylation type 1F?

  • Congenital disorder of glycosylation type 1F: 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 IF is caused by a defect on chromosome 17p13.1-p12 and involves a defect on the MPDU1 gene.

Congenital disorder of glycosylation type 1F: Introduction

Types of Congenital disorder of glycosylation type 1F:

Broader types of Congenital disorder of glycosylation type 1F:

What causes Congenital disorder of glycosylation type 1F?

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

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

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

Congenital disorder of glycosylation type 1F: Testing

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

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

How is it treated?

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

Name and Aliases of Congenital disorder of glycosylation type 1F

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

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

CDG If, CDG1f

 

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