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Craniofacial dysostosis type 1

Craniofacial dysostosis type 1: Introduction

Craniofacial dysostosis type 1: A rare genetic disorder characterized by premature joining of certain skull bones during development which has an impact on the shape of the head and face. Features include poor vision, hypoplasia of maxilla an impaired hearing. More detailed information about the symptoms, causes, and treatments of Craniofacial dysostosis type 1 is available below.

Symptoms of Craniofacial dysostosis type 1

Home Diagnostic Testing

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Craniofacial dysostosis type 1: Complications

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Causes of Craniofacial dysostosis type 1

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Disease Topics Related To Craniofacial dysostosis type 1

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Less Common Symptoms of Craniofacial dysostosis type 1

Craniofacial dysostosis type 1: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Craniofacial dysostosis type 1: Research Doctors & Specialists

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Craniofacial dysostosis type 1: Animations

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Craniofacial dysostosis type 1: Broader Related Topics

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Definitions of Craniofacial dysostosis type 1:

Craniofacial dysostosis type 1 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Craniofacial dysostosis type 1, or a subtype of Craniofacial dysostosis type 1, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Related Craniofacial dysostosis type 1 Info

More information about Craniofacial dysostosis type 1

  1. Craniofacial dysostosis type 1: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
  7. Complications
 

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