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Osteogenesis imperfecta type IV

Osteogenesis imperfecta type IV: Introduction

Osteogenesis imperfecta type IV: A rare genetic connective tissue disorder characterized by fragile bones and blue sclerae. The osteoporosis tends to be moderate and there is generally no joint hyperextensibility. More detailed information about the symptoms, causes, and treatments of Osteogenesis imperfecta type IV is available below.

Symptoms of Osteogenesis imperfecta type IV

Home Diagnostic Testing

Home medical testing related to Osteogenesis imperfecta type IV:

Wrongly Diagnosed with Osteogenesis imperfecta type IV?

Osteogenesis imperfecta type IV: Deaths

Read more about Deaths and Osteogenesis imperfecta type IV.

Osteogenesis imperfecta type IV: Complications

Review possible medical complications related to Osteogenesis imperfecta type IV:

Causes of Osteogenesis imperfecta type IV

Read more about causes of Osteogenesis imperfecta type IV.

Disease Topics Related To Osteogenesis imperfecta type IV

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

Osteogenesis imperfecta type IV: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Osteogenesis imperfecta type IV

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Osteogenesis imperfecta type IV: Research Doctors & Specialists

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Other doctor, physician and specialist research services:

Hospitals & Clinics: Osteogenesis imperfecta type IV

Research quality ratings and patient safety measures for medical facilities in specialties related to Osteogenesis imperfecta type IV:

Choosing the Best Hospital: More general information, not necessarily in relation to Osteogenesis imperfecta type IV, on hospital performance and surgical care quality:

Osteogenesis imperfecta type IV: Animations

Statistics for Osteogenesis imperfecta type IV

Osteogenesis imperfecta type IV: Broader Related Topics

User Interactive Forums

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Definitions of Osteogenesis imperfecta type IV:

Osteogenesis imperfecta type IV 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 IV, or a subtype of Osteogenesis imperfecta type IV, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Related Osteogenesis imperfecta type IV Info

More information about Osteogenesis imperfecta type IV

  1. Osteogenesis imperfecta type IV: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
  7. Deaths
  8. Complications
 

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