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Carbohydrate deficiency glycoprotein syndrome type II

Carbohydrate deficiency glycoprotein syndrome type II: Introduction

Carbohydrate deficiency glycoprotein syndrome type II: 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 2 is caused by a genetic defect which involves the gene for a particular enzyme (Golgi localized N-acetyl-glucosaminyltransferase II). Type 2 tends to have more severe psychomotor retardation than type 1 but there is no peripheral neuropathy or underdeveloped cerebellum. More detailed information about the symptoms, causes, and treatments of Carbohydrate deficiency glycoprotein syndrome type II is available below.

Symptoms of Carbohydrate deficiency glycoprotein syndrome type II

Wrongly Diagnosed with Carbohydrate deficiency glycoprotein syndrome type II?

Causes of Carbohydrate deficiency glycoprotein syndrome type II

Read more about causes of Carbohydrate deficiency glycoprotein syndrome type II.

Misdiagnosis and Carbohydrate deficiency glycoprotein syndrome type II

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More information about Carbohydrate deficiency glycoprotein syndrome type II

  1. Carbohydrate deficiency glycoprotein syndrome type II: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
 

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