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Pfeiffer syndrome

Pfeiffer syndrome: Introduction

Pfeiffer syndrome: A rare genetic disorder where some of the skull bones fuse too early which affects the size and shape of the skull and face. Thumb and toe abnormalities are also present. There are three types of Pfeiffer syndrome with varying degrees of severity. More detailed information about the symptoms, causes, and treatments of Pfeiffer syndrome is available below.

Symptoms of Pfeiffer syndrome

Home Diagnostic Testing

Home medical testing related to Pfeiffer syndrome:

Wrongly Diagnosed with Pfeiffer syndrome?

Pfeiffer syndrome: Complications

Read more about complications of Pfeiffer syndrome.

Causes of Pfeiffer syndrome

Read more about causes of Pfeiffer syndrome.

Disease Topics Related To Pfeiffer syndrome

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

Pfeiffer syndrome: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Pfeiffer syndrome

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Pfeiffer syndrome: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Evidence Based Medicine Research for Pfeiffer syndrome

Medical research articles related to Pfeiffer syndrome include:

Click here to find more evidence-based articles on the TRIP Database

Pfeiffer syndrome: Animations

Research about Pfeiffer syndrome

Visit our research pages for current research about Pfeiffer syndrome treatments.

Statistics for Pfeiffer syndrome

Pfeiffer syndrome: Broader Related Topics

User Interactive Forums

Read about other experiences, ask a question about Pfeiffer syndrome, or answer someone else's question, on our message boards:

Definitions of Pfeiffer syndrome:

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

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

Related Pfeiffer syndrome Info

More information about Pfeiffer syndrome

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

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