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Congenital disorder of glycosylation type 2E

Congenital disorder of glycosylation type 2E: Introduction

Congenital disorder of glycosylation type 2E: 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 2e is caused by a defect on chromosome 16p and involves a defect in the gene for oligomeric complex-7. More detailed information about the symptoms, causes, and treatments of Congenital disorder of glycosylation type 2E is available below.

Symptoms of Congenital disorder of glycosylation type 2E

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Causes of Congenital disorder of glycosylation type 2E

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Congenital disorder of glycosylation type 2E: Undiagnosed Conditions

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Misdiagnosis and Congenital disorder of glycosylation type 2E

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 symptoms. Although the most common symptoms are anal...read more »

Mesenteric adenitis misdiagnosed as appendicitis in children: Because appendicitis is one of the more feared conditions for a child with abdominal pain, it...read more »

Blood pressure cuffs misdiagnose hypertension in children: One known misdiagnosis issue with hyperension, arises in relation to the simple equipment used to test blood pressure. The "cuff"...read more »

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. See misdiagnosis of migraine...read more »

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More information about Congenital disorder of glycosylation type 2E

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

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