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Osteopetrosis autosomal dominant type 2

Osteopetrosis autosomal dominant type 2: Introduction

Osteopetrosis autosomal dominant type 2: A very rare dominantly inherited syndrome characterized mainly by increased bone density that affects mostly the spine, pelvis and base of the skull. The increased bone density results because old bone is not resorbed and replaced with new bone. More detailed information about the symptoms, causes, and treatments of Osteopetrosis autosomal dominant type 2 is available below.

Symptoms of Osteopetrosis autosomal dominant type 2

Home Diagnostic Testing

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Wrongly Diagnosed with Osteopetrosis autosomal dominant type 2?

Osteopetrosis autosomal dominant type 2: Related Patient Stories

Osteopetrosis autosomal dominant type 2: Deaths

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Osteopetrosis autosomal dominant type 2: Complications

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Causes of Osteopetrosis autosomal dominant type 2

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Osteopetrosis autosomal dominant type 2: Research Doctors & Specialists

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Statistics for Osteopetrosis autosomal dominant type 2

Osteopetrosis autosomal dominant type 2: Broader Related Topics

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Definitions of Osteopetrosis autosomal dominant type 2:

Osteopetrosis autosomal dominant type 2 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Osteopetrosis autosomal dominant type 2, or a subtype of Osteopetrosis autosomal dominant type 2, 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 Osteopetrosis autosomal dominant type 2 as a "rare disease".
Source - Orphanet

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More information about Osteopetrosis autosomal dominant type 2

  1. Osteopetrosis autosomal dominant type 2: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Home Testing
  6. Deaths
  7. Complications
 

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