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Glycine synthase deficiency, type 2

Glycine synthase deficiency, type 2: Introduction

Glycine synthase deficiency, type 2: A rare genetic disorder characterized by high blood glycine levels. It is caused by a defect in the T protein (tetrahydrofolate-requiring enzyme) in the energy creating center of cells (mitochondria). More detailed information about the symptoms, causes, and treatments of Glycine synthase deficiency, type 2 is available below.

Symptoms of Glycine synthase deficiency, type 2

Wrongly Diagnosed with Glycine synthase deficiency, type 2?

Causes of Glycine synthase deficiency, type 2

Read more about causes of Glycine synthase deficiency, type 2.

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Misdiagnosis and Glycine synthase deficiency, type 2

Vitamin B12 deficiency under-diagnosed: The condition of Vitamin B12 deficiency is a possible misdiagnosis of various conditions, such as multiple sclerosis (see symptoms of multiple sclerosis). See symptoms of Vitamin B12...read more »

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More information about Glycine synthase deficiency, type 2

  1. Glycine synthase deficiency, type 2: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
 

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