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Glycine synthase deficiency, type 1

Glycine synthase deficiency, type 1: Introduction

Glycine synthase deficiency, type 1: A rare genetic disorder characterized by high blood glycine levels. It is caused by a defect in the P protein (pyridoxal phosphate-dependent glycine decarboxylase) in the energy creating center of cells (mitochondria). More detailed information about the symptoms, causes, and treatments of Glycine synthase deficiency, type 1 is available below.

Symptoms of Glycine synthase deficiency, type 1

Wrongly Diagnosed with Glycine synthase deficiency, type 1?

Causes of Glycine synthase deficiency, type 1

Read more about causes of Glycine synthase deficiency, type 1.

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Misdiagnosis and Glycine synthase deficiency, type 1

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More information about Glycine synthase deficiency, type 1

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

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