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Congenital disorder of glycosylation type 2F

Congenital disorder of glycosylation type 2F: Introduction

Congenital disorder of glycosylation type 2F: 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 IIf is caused by a defect on chromosome 6q25.16q15 and involves a defect on the gene for CMP-sialic acid transporter. More detailed information about the symptoms, causes, and treatments of Congenital disorder of glycosylation type 2F is available below.

Symptoms of Congenital disorder of glycosylation type 2F

Home Diagnostic Testing

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Congenital disorder of glycosylation type 2F: Complications

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Causes of Congenital disorder of glycosylation type 2F

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Congenital disorder of glycosylation type 2F: Undiagnosed Conditions

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Misdiagnosis and Congenital disorder of glycosylation type 2F

Mild worm infections undiagnosed in children: Human worm infestations, esp. threadworm, can be overlooked in some cases, because it may cause only mild or even absent...read more »

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Children with migraine often misdiagnosed: A migraine often fails to be correctly diagnosed in pediatric patients. These patients are not the typical migraine sufferers, but migraines can also occur in children....read more »

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More information about Congenital disorder of glycosylation type 2F

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

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