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Osteolysis hereditary multicentric

Osteolysis hereditary multicentric: Introduction

Osteolysis hereditary multicentric: A very rare skeletal disorder characterized by bone loss in the hand and foot bones (carpals and tarsals) as well as abnormalities involving the long bones and digits. More detailed information about the symptoms, causes, and treatments of Osteolysis hereditary multicentric is available below.

Symptoms of Osteolysis hereditary multicentric

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Osteolysis hereditary multicentric: Complications

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Causes of Osteolysis hereditary multicentric

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Definitions of Osteolysis hereditary multicentric:

Osteolysis hereditary multicentric is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Osteolysis hereditary multicentric, or a subtype of Osteolysis hereditary multicentric, 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 Osteolysis hereditary multicentric as a "rare disease".
Source - Orphanet

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More information about Osteolysis hereditary multicentric

  1. Osteolysis hereditary multicentric: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Home Testing
  6. Complications
 

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