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
See full list of 21
symptoms of Craniofacial dysostosis type 1
Home Diagnostic Testing
Home medical testing related to Craniofacial dysostosis type 1:
- Ear Infections: Home Testing:
- Vision & Eye Health: Home Testing:
- more...»
Wrongly Diagnosed with Craniofacial dysostosis type 1?
Craniofacial dysostosis type 1: Complications
Review possible medical complications related to Craniofacial dysostosis type 1:
Causes of Craniofacial dysostosis type 1
Read more about causes of Craniofacial dysostosis type 1.
Disease Topics Related To Craniofacial dysostosis type 1
Research the causes of these diseases that are similar to, or related to, Craniofacial dysostosis type 1:
Less Common Symptoms of Craniofacial dysostosis type 1
See full list of 12
occasional 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
Research related physicians and medical specialists:
- Face / Facial / Oral Health Specialists:
- Ear, Nose & Throat Specialists:
- Eye Health Specialists (Ophthalmology):
- more specialists...»
Other doctor, physician and specialist research services:
Craniofacial dysostosis type 1: Animations
More Craniofacial dysostosis type 1 animations & videos
Statistics for Craniofacial dysostosis type 1
Craniofacial dysostosis type 1: Broader Related Topics
Types of Craniofacial dysostosis type 1
User Interactive Forums
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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)
Contents for Craniofacial dysostosis type 1: