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Hyperprolinemia type 2

Hyperprolinemia type 2: Introduction

Hyperprolinemia type 2: A rare metabolic abnormality involving a deficiency of a particular enzyme (Delta-1-pyrroline-5-carboxylate dehydrogenase) which affects amino acid metabolism and causes mental retardation and convulsions. More detailed information about the symptoms, causes, and treatments of Hyperprolinemia type 2 is available below.

Symptoms of Hyperprolinemia type 2

Home Diagnostic Testing

Home medical testing related to Hyperprolinemia type 2:

Wrongly Diagnosed with Hyperprolinemia type 2?

Causes of Hyperprolinemia type 2

Read more about causes of Hyperprolinemia type 2.

Misdiagnosis and Hyperprolinemia type 2

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Hyperprolinemia type 2: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Hyperprolinemia type 2: Animations

Statistics for Hyperprolinemia type 2

Hyperprolinemia type 2: Broader Related Topics

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Definitions of Hyperprolinemia type 2:

Hyperprolinemia type 2 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Hyperprolinemia type 2, or a subtype of Hyperprolinemia type 2, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Related Hyperprolinemia type 2 Info

More information about Hyperprolinemia type 2

  1. Hyperprolinemia type 2: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
 

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