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Pfeiffer syndrome Type 2

Pfeiffer syndrome Type 2: Introduction

Pfeiffer syndrome Type 2: A rare genetic disorder characterized by premature joining of certain skull bones during development which has an impact on the shape of the head and face. Features include craniofacial and cardiovascular malformations with death often occurring early. More detailed information about the symptoms, causes, and treatments of Pfeiffer syndrome Type 2 is available below.

Symptoms of Pfeiffer syndrome Type 2

Home Diagnostic Testing

Home medical testing related to Pfeiffer syndrome Type 2:

Wrongly Diagnosed with Pfeiffer syndrome Type 2?

Pfeiffer syndrome Type 2: Deaths

Read more about Deaths and Pfeiffer syndrome Type 2.

Pfeiffer syndrome Type 2: Complications

Review possible medical complications related to Pfeiffer syndrome Type 2:

Causes of Pfeiffer syndrome Type 2

Read more about causes of Pfeiffer syndrome Type 2.

Disease Topics Related To Pfeiffer syndrome Type 2

Research the causes of these diseases that are similar to, or related to, Pfeiffer syndrome Type 2:

Pfeiffer syndrome Type 2: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Pfeiffer syndrome Type 2

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

Pfeiffer syndrome Type 2: Research Doctors & Specialists

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Other doctor, physician and specialist research services:

Pfeiffer syndrome Type 2: Animations

Pfeiffer syndrome Type 2: Broader Related Topics

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Related Pfeiffer syndrome Type 2 Info

More information about Pfeiffer syndrome Type 2

  1. Pfeiffer syndrome Type 2: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
  7. Deaths
  8. Complications
 

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