Crouzons syndrome- A rare genetic disorder


Article PDF :

Veiw Full Text PDF

Article type :

Case Report

Author :

Babita Niranjan, Ashutosh Dubey, Nikita Agrawal, Raj Mourya, N D Shashikiran, Mylavarapu Krishna Sagar

Volume :

6

Issue :

2

Abstract :

Background: Crouzon syndrome is a rare genetic autosomal dominant disorder characterized by distinctive malformations of the skull and cranio-facial region. Case Description: The parents of a 7 years old boy reported with a complaint of pain in the upper front and back teeth region since 3-4months. He also presented with typical features of craniofacial deformity, maxillary hypoplasia, exophthalmos, hypertelosrism, ptosis are present among other manifestations. The overall presentation gave an indication towards a clinical diagnosis of Crouzon’s syndrome. This case report describes the different clinical features and management under general anesthesia of a pediatric patient who reported with characteristic findings of this syndrome. Conclusion: This case report emphasizes the important role of a pediatric dentist in diagnosing such syndrome and to provide corrective measure along with co-ordination of a multi-disciplinary team. The team may comprise a geneticist, neurosurgeon, psychologist, speech and language therapist, nose surgeons and respiratory care specialist.

Keyword :

 Crouzon, Cranio-facial deformity, Autosomal dominant disorder.
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