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Quintessence Publishing: Journals: QI
Quintessence International

Edited by Eli Eliav

ISSN 0033-6572 (print) • ISSN 1936-7163 (online)

June 1999
Volume 30 , Issue 6

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Apert syndrome: A case report with discussion of craniofacial features

Rajesh P. Paravatty, BDS/Auswaf Ahsan, BDS/Bastian T. Sebastian, MDS/Keerthilatha M. Pai, MDS/Promod K. Dayal, MDS

Pages: 423-426
PMID: 10635279

Apert syndrome is a rare congenital anomaly characterized by acrocephaly, syndactyly, and abnormalities of other organs. It has characteristic features in the orofacial region, affecting the eyes, palate, middle third of face, and uvula. In this case report, the features of Apert syndrome, particularly in relation to the orofacial region, are discussed.

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