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Crouzon syndrome: clinico-radiological illustration of a case
Raviprakash Sasankoti Mohan1, Naveen Shanker Vemanna, Sankalp Verma
1Department of Oral Medicine Diagnosis and Radiology, Kothiwal Dental College and Research Centre, Mora Mustaqueem, Moradabad, Uttar Pradesh, India.
Abstract:
Crouzon syndrome, also called craniofacial dysostosis, is an autosomal dominant disorder with complete penetrance and variable expressivity. Described by a French neurosurgeon in 1912, it is a rare genetic disorder characterized by premature closure of cranial sutures, midfacial hypoplasia, and orbital defects. Here, we report a case of this rare entity. The patient presented with brachycephaly, maxillary hypoplasia, exophthalmos, mandibular prognathism, along with dental and orbital abnormalities.
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