Crouzons syndrome

Crouzons syndrome --> craniofacial dysostosis

(Science: paediatrics) a genetic disorder (autosomal dominant) characterised by abnormalities of the cranial sutures, widening of the skull, a high forehead, ocular hypertelorism, exophthalmos, beaked nose and hypoplasia of the maxilla

Inheritance: autosomal dominant.

Retrieved from ""
First | Previous (Crouzon syndrome) | Next (Crowding) | Last
Please contribute to this project, if you have more information about this term feel free to edit this page.