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Craniometaphyseal dysplasia dominant type

Craniometaphyseal dysplasia dominant type: Introduction

Craniometaphyseal dysplasia dominant type: A rare genetic disorder characterized by head and facial abnormalities as well as mild limb abnormalities. Increased cranial pressure can lead to further complications. More detailed information about the symptoms, causes, and treatments of Craniometaphyseal dysplasia dominant type is available below.

Symptoms of Craniometaphyseal dysplasia dominant type

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Craniometaphyseal dysplasia dominant type: Deaths

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Craniometaphyseal dysplasia dominant type: Complications

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Causes of Craniometaphyseal dysplasia dominant type

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Disease Topics Related To Craniometaphyseal dysplasia dominant type

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Craniometaphyseal dysplasia dominant type: Broader Related Topics

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Definitions of Craniometaphyseal dysplasia dominant type:

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

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More information about Craniometaphyseal dysplasia dominant type

  1. Craniometaphyseal dysplasia dominant type: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Deaths
  6. Complications
 

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