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Phosphoglycerate Kinase Deficiency

Phosphoglycerate Kinase Deficiency: Introduction

Phosphoglycerate Kinase Deficiency: A condition which is characterized by a deficiency in the enzyme phosphoglycerate kinase. More detailed information about the symptoms, causes, and treatments of Phosphoglycerate Kinase Deficiency is available below.

Symptoms of Phosphoglycerate Kinase Deficiency

Wrongly Diagnosed with Phosphoglycerate Kinase Deficiency?

Phosphoglycerate Kinase Deficiency: Related Patient Stories

Phosphoglycerate Kinase Deficiency: Complications

Read more about complications of Phosphoglycerate Kinase Deficiency.

Causes of Phosphoglycerate Kinase Deficiency

Read more about causes of Phosphoglycerate Kinase Deficiency.

Disease Topics Related To Phosphoglycerate Kinase Deficiency

Research the causes of these diseases that are similar to, or related to, Phosphoglycerate Kinase Deficiency:

Misdiagnosis and Phosphoglycerate Kinase Deficiency

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 more »

Phosphoglycerate Kinase Deficiency: Research Doctors & Specialists

Research related physicians and medical specialists:

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Evidence Based Medicine Research for Phosphoglycerate Kinase Deficiency

Medical research articles related to Phosphoglycerate Kinase Deficiency include:

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Phosphoglycerate Kinase Deficiency: Animations

Research about Phosphoglycerate Kinase Deficiency

Visit our research pages for current research about Phosphoglycerate Kinase Deficiency treatments.

Phosphoglycerate Kinase Deficiency: Broader Related Topics

User Interactive Forums

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Definitions of Phosphoglycerate Kinase Deficiency:

Phosphoglycerate kinase (E.C. deficiency with chronic nonspherocytic hemolytic anemia and variable neurologic and myopathic features in males or occasional hemolysis without any neurological complications. Variability of expression is believed to be due to biochemical properties of PKG variants. - (Source - Diseases Database)


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