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Phenylketonuria type 2

Phenylketonuria type 2: Introduction

Phenylketonuria type 2: A genetic condition where phenylalanine (component of protein) is unable to be broken down due to an enzyme (phenylalanine hydroxylase) deficiency which leads to a harmful build up of the compound. The condition is characterized by neurological symptoms as well as the presence of increased levels of phenylalanine in the blood. More detailed information about the symptoms, causes, and treatments of Phenylketonuria type 2 is available below.

Symptoms of Phenylketonuria type 2

Home Diagnostic Testing

Home medical testing related to Phenylketonuria type 2:

Wrongly Diagnosed with Phenylketonuria type 2?

Phenylketonuria type 2: Complications

Read more about complications of Phenylketonuria type 2.

Causes of Phenylketonuria type 2

Read more about causes of Phenylketonuria type 2.

Disease Topics Related To Phenylketonuria type 2

Research the causes of these diseases that are similar to, or related to, Phenylketonuria type 2:

Phenylketonuria type 2: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Phenylketonuria type 2

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Phenylketonuria type 2: Research Doctors & Specialists

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Statistics for Phenylketonuria type 2

Phenylketonuria type 2: Broader Related Topics

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Definitions of Phenylketonuria type 2:

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Phenylketonuria type 2 as a "rare disease".
Source - Orphanet

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More information about Phenylketonuria type 2

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

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