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Pfeiffer-Palm-Teller syndrome

Pfeiffer-Palm-Teller syndrome: Introduction

Pfeiffer-Palm-Teller syndrome: A rare disorder characterized by facial peculiarities, defective tooth enamel and progressive joint stiffness. More detailed information about the symptoms, causes, and treatments of Pfeiffer-Palm-Teller syndrome is available below.

Symptoms of Pfeiffer-Palm-Teller syndrome

Wrongly Diagnosed with Pfeiffer-Palm-Teller syndrome?

Pfeiffer-Palm-Teller syndrome: Related Patient Stories

Causes of Pfeiffer-Palm-Teller syndrome

Read more about causes of Pfeiffer-Palm-Teller syndrome.

Disease Topics Related To Pfeiffer-Palm-Teller syndrome

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

Misdiagnosis and Pfeiffer-Palm-Teller syndrome

Psoriatic arthritis often undiagnosed cause of joint conditions: Patients with the skin condition psoriasis can also have the related arthritis subtype called " psoriatic...read more »

Pfeiffer-Palm-Teller syndrome: Research Doctors & Specialists

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Hospitals & Clinics: Pfeiffer-Palm-Teller syndrome

Research quality ratings and patient safety measures for medical facilities in specialties related to Pfeiffer-Palm-Teller syndrome:

Choosing the Best Hospital: More general information, not necessarily in relation to Pfeiffer-Palm-Teller syndrome, on hospital performance and surgical care quality:

Statistics for Pfeiffer-Palm-Teller syndrome

Pfeiffer-Palm-Teller syndrome: Broader Related Topics

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Definitions of Pfeiffer-Palm-Teller syndrome:

Pfeiffer-Palm-Teller 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-Palm-Teller syndrome, or a subtype of Pfeiffer-Palm-Teller 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-Palm-Teller syndrome as a "rare disease".
Source - Orphanet

 

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