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Ollier Disease

Ollier Disease: Introduction

Ollier Disease: A rare genetic disorder characterized by abnormal bone development. More detailed information about the symptoms, causes, and treatments of Ollier Disease is available below.

Symptoms of Ollier Disease

Wrongly Diagnosed with Ollier Disease?

Ollier Disease: Related Patient Stories

Ollier Disease: Complications

Review possible medical complications related to Ollier Disease:

Causes of Ollier Disease

Read more about causes of Ollier Disease.

Disease Topics Related To Ollier Disease

Research the causes of these diseases that are similar to, or related to, Ollier Disease:

Evidence Based Medicine Research for Ollier Disease

Medical research articles related to Ollier Disease include:

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

Research about Ollier Disease

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Statistics for Ollier Disease

Ollier Disease: Broader Related Topics

User Interactive Forums

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

Definitions of Ollier Disease:

Benign growths of cartilage in the metaphyses of several bones. - (Source - Diseases Database)

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

Related Ollier Disease Info

Videos about Ollier Disease

 

Forum Discussions about Ollier Disease

More information about Ollier Disease

  1. Ollier Disease: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Complications
 

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