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Congenital disorder of glycosylation type 1X

Congenital disorder of glycosylation type 1X: Introduction

Congenital disorder of glycosylation type 1X: Congenital disorder of glycosylation is a rare inherited metabolic disorder where defective carbohydrate compounds are attached to glycoproteins and thus impairing glycoprotein function. Type 1X also involves thrombocytopenia with normal levels of phosphomannomutase and phosphomannose isomerase. This form of the condition is severe and results in death during infancy. More detailed information about the symptoms, causes, and treatments of Congenital disorder of glycosylation type 1X is available below.

Symptoms of Congenital disorder of glycosylation type 1X

Home Diagnostic Testing

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Causes of Congenital disorder of glycosylation type 1X

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Congenital disorder of glycosylation type 1X: Undiagnosed Conditions

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Misdiagnosis and Congenital disorder of glycosylation type 1X

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...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...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 simply...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 1X

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

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