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Congenital disorder of glycosylation type 1C

Congenital disorder of glycosylation type 1C: Introduction

Congenital disorder of glycosylation type 1C: A very rare inherited metabolic disorder where defective carbohydrate compounds are attached to glycoproteins and thus impairing glycoprotein function. Type 1C has a ?1,3-glucosyl-transferase enzyme defect. More detailed information about the symptoms, causes, and treatments of Congenital disorder of glycosylation type 1C is available below.

Symptoms of Congenital disorder of glycosylation type 1C

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Causes of Congenital disorder of glycosylation type 1C

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Disease Topics Related To Congenital disorder of glycosylation type 1C

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Less Common Symptoms of Congenital disorder of glycosylation type 1C

Congenital disorder of glycosylation type 1C: Undiagnosed Conditions

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Misdiagnosis and Congenital disorder of glycosylation type 1C

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...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 over-diagnosed (it can, of course, also fail to be diagnosed with fatal...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 arm to measure blood pressure can...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...read more »

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More information about Congenital disorder of glycosylation type 1C

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

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