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Osteopetrosis autosomal dominant type 1

Osteopetrosis autosomal dominant type 1: Introduction

Osteopetrosis autosomal dominant type 1: A very rare dominantly inherited syndrome characterized mainly by increased bone density. The increased bone density results because old bone is not resorbed and replaced with new bone. Only 33 cases in 3 families have been reported. In type I, the increased bone density occurs throughout the body with the skull being the most affected. There is no associated increase in risk of fractures. Many cases are asymptomatic. More detailed information about the symptoms, causes, and treatments of Osteopetrosis autosomal dominant type 1 is available below.

Symptoms of Osteopetrosis autosomal dominant type 1

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Osteopetrosis autosomal dominant type 1: Deaths

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Causes of Osteopetrosis autosomal dominant type 1

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Definitions of Osteopetrosis autosomal dominant type 1:

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 1 as a "rare disease".
Source - Orphanet

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More information about Osteopetrosis autosomal dominant type 1

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

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