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Crouzon disease (medical condition): A rare genetic disorder characterized by premature joining of certain...more »
See also:
Craniofacial dysostosis type 1:
»Introduction: Craniofacial dysostosis type 1
»Symptoms of Craniofacial dysostosis type 1
These medical condition or symptom topics may be relevant to medical information for Crouzon disease:
Crouzon disease is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Crouzon disease, or a subtype of Crouzon disease,
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 if affects 1 person per 2,000.
They list Crouzon disease as a "rare disease".
Source - Orphanet
Crouzon disease: Another name for Craniofacial dysostosis type 1 (or close medical condition association).
»Introduction: Craniofacial dysostosis type 1
»Symptoms of Craniofacial dysostosis type 1
Crouzon disease: Crouzon disease is listed as a type of (or associated with) the following medical conditions in our database:
Some of the symptoms of Crouzon disease incude:
See full list of 21 symptoms of Crouzon disease (Craniofacial dysostosis type 1)
These medical disease topics may be related to Crouzon disease:
Source - NIH
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