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What is Congenital Disorder of Glycosylation, Type 1o?

What is Congenital Disorder of Glycosylation, Type 1o?

  • Congenital Disorder of Glycosylation, Type 1o: A very rare inherited metabolic disorder where defective carbohydrate compounds are attached to glycoproteins and thus impairing glycoprotein function. Type 1O has a defect in the DPM3 gene which results in decreased activity of an enzyme called dolichol-phosphage-mannose (Dol-P-M).

Congenital Disorder of Glycosylation, Type 1o: Introduction

Types of Congenital Disorder of Glycosylation, Type 1o:

Broader types of Congenital Disorder of Glycosylation, Type 1o:

What causes Congenital Disorder of Glycosylation, Type 1o?

Causes of Congenital Disorder of Glycosylation, Type 1o: see causes of Congenital Disorder of Glycosylation, Type 1o

What are the symptoms of Congenital Disorder of Glycosylation, Type 1o?

Symptoms of Congenital Disorder of Glycosylation, Type 1o: see symptoms of Congenital Disorder of Glycosylation, Type 1o

Congenital Disorder of Glycosylation, Type 1o: Testing

Diagnostic testing: see tests for Congenital Disorder of Glycosylation, Type 1o.

Misdiagnosis: see misdiagnosis and Congenital Disorder of Glycosylation, Type 1o.

How is it treated?

Treatments for Congenital Disorder of Glycosylation, Type 1o: see treatments for Congenital Disorder of Glycosylation, Type 1o

Name and Aliases of Congenital Disorder of Glycosylation, Type 1o

Main name of condition: Congenital Disorder of Glycosylation, Type 1o

Other names or spellings for Congenital Disorder of Glycosylation, Type 1o:

CDG1O

 

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