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
See full list of 23
symptoms of Pyle disease
Home Diagnostic Testing
Home medical testing related to Pyle disease:
- Ear Infections: Home Testing:
- Vision & Eye Health: Home Testing:
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
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
More Pyle disease animations & videos
Statistics for Pyle disease
Pyle disease: Broader Related Topics
Types of Pyle disease
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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