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Pyle disease

Pyle disease: Introduction

Pyle disease: A rare genetic disorder characterized by numerous bone abnormalities as well as loss of vision and hearing. More detailed information about the symptoms, causes, and treatments of Pyle disease is available below.

Symptoms of Pyle disease

Home Diagnostic Testing

Home medical testing related to Pyle disease:

Wrongly Diagnosed with Pyle disease?

Pyle disease: Related Patient Stories

Pyle disease: Complications

Review possible medical complications related to Pyle disease:

Causes of Pyle disease

Read more about causes of Pyle disease.

Pyle disease: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Pyle disease: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Pyle disease: Animations

Statistics for Pyle disease

Pyle disease: Broader Related Topics

User Interactive Forums

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Definitions of Pyle disease:

Pyle disease is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Pyle disease, or a subtype of Pyle disease, 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 Pyle disease as a "rare disease".
Source - Orphanet

 

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