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Osteogenesis imperfecta Type I

Osteogenesis imperfecta Type I: Introduction

Osteogenesis imperfecta Type I: A rare genetic connective tissue disorder characterized by fragile bones, blue sclerae and hyperextensible joints. More detailed information about the symptoms, causes, and treatments of Osteogenesis imperfecta Type I is available below.

Symptoms of Osteogenesis imperfecta Type I

Home Diagnostic Testing

Home medical testing related to Osteogenesis imperfecta Type I:

Wrongly Diagnosed with Osteogenesis imperfecta Type I?

Osteogenesis imperfecta Type I: Related Patient Stories

Osteogenesis imperfecta Type I: Deaths

Read more about Deaths and Osteogenesis imperfecta Type I.

Causes of Osteogenesis imperfecta Type I

Read more about causes of Osteogenesis imperfecta Type I.

Disease Topics Related To Osteogenesis imperfecta Type I

Research the causes of these diseases that are similar to, or related to, Osteogenesis imperfecta Type I:

Osteogenesis imperfecta Type I: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Osteogenesis imperfecta Type I

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

Osteogenesis imperfecta Type I: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Evidence Based Medicine Research for Osteogenesis imperfecta Type I

Medical research articles related to Osteogenesis imperfecta Type I include:

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

Osteogenesis imperfecta Type I: Animations

Research about Osteogenesis imperfecta Type I

Visit our research pages for current research about Osteogenesis imperfecta Type I treatments.

Statistics for Osteogenesis imperfecta Type I

Osteogenesis imperfecta Type I: Broader Related Topics

User Interactive Forums

Read about other experiences, ask a question about Osteogenesis imperfecta Type I, or answer someone else's question, on our message boards:

Definitions of Osteogenesis imperfecta Type I:

Osteogenesis imperfecta Type I is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Osteogenesis imperfecta Type I, or a subtype of Osteogenesis imperfecta Type I, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

 

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