Craniofacial abnormalities

A syndrome inherited in an autosomal dominant pattern. It is characterized by early fusion of the bones of the skull and face. Patients have a distinctive facial appearance which includes low-set ears, brachycephaly, hypertelorism, exophthalmos, and mandibular prognathism.

Disease Alternative Name

craniofacial dysostosis
crouzon syndrome
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Consulting Physician

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