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Congenital disorder of glycosylation type 1I

Congenital disorder of glycosylation type 1I: Introduction

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. More detailed information about the symptoms, causes, and treatments of Congenital disorder of glycosylation type 1I is available below.

Symptoms of Congenital disorder of glycosylation type 1I

Home Diagnostic Testing

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Causes of Congenital disorder of glycosylation type 1I

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Congenital disorder of glycosylation type 1I: Undiagnosed Conditions

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Misdiagnosis and Congenital disorder of glycosylation type 1I

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...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 can be...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" around the...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...read more »

Congenital disorder of glycosylation type 1I: Research Doctors & Specialists

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More information about Congenital disorder of glycosylation type 1I

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

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