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Progressive Osseous Heteroplasia

Progressive Osseous Heteroplasia: Introduction

Progressive Osseous Heteroplasia: A very rare disorder where bone forms in abnormal parts of the body such as the skin. The extent and location of the abnormal bone formation is variable. More detailed information about the symptoms, causes, and treatments of Progressive Osseous Heteroplasia is available below.

Symptoms of Progressive Osseous Heteroplasia

  • Patches of bone formation on skin
  • Bone formation in deep connective tissue
  • Bone formation in fat layer of skin
  • Bone formation in muscles
  • Bone formation in tendons
  • more symptoms...»

Wrongly Diagnosed with Progressive Osseous Heteroplasia?

Progressive Osseous Heteroplasia: Related Patient Stories

Causes of Progressive Osseous Heteroplasia

Read more about causes of Progressive Osseous Heteroplasia.

Disease Topics Related To Progressive Osseous Heteroplasia

Research the causes of these diseases that are similar to, or related to, Progressive Osseous Heteroplasia:

Misdiagnosis and Progressive Osseous Heteroplasia

Psoriasis often undiagnosed cause of skin symptoms in children: Children who suffer from the skin disorder called psoriasis can often go undiagnosed. The main problem is that psoriasis is rare in children, and more »

Progressive Osseous Heteroplasia: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Evidence Based Medicine Research for Progressive Osseous Heteroplasia

Medical research articles related to Progressive Osseous Heteroplasia include:

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

Progressive Osseous Heteroplasia: Animations

Research about Progressive Osseous Heteroplasia

Visit our research pages for current research about Progressive Osseous Heteroplasia treatments.

Statistics for Progressive Osseous Heteroplasia

Progressive Osseous Heteroplasia: Broader Related Topics

User Interactive Forums

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Definitions of Progressive Osseous Heteroplasia:

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


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