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Crouzon disease

Introduction: Crouzon disease

Description of Crouzon disease

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

Crouzon disease: Related Topics

These medical condition or symptom topics may be relevant to medical information for Crouzon disease:

Crouzon disease: Rare Disease

Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

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

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 as a Disease

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: Related Diseases

Crouzon disease: Crouzon disease is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of Crouzon disease (Craniofacial dysostosis type 1)

Some of the symptoms of Crouzon disease incude:

Crouzon disease: Related Disease Topics

These medical disease topics may be related to Crouzon disease:

Terms associated with Crouzon disease:

Terms Similar to Crouzon disease:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

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