Apert syndrome: A case report with discussion of craniofacial features

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

Research output: Contribution to journalArticle

11 Citations (Scopus)

Abstract

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.

Original languageEnglish
Pages (from-to)423-426
Number of pages4
JournalQuintessence International
Volume30
Issue number6
Publication statusPublished - 01-06-1999

All Science Journal Classification (ASJC) codes

  • Dentistry(all)

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    Paravatty, R. P., Ahsan, A., Sebastian, B. T., Pai, K. M., & Dayal, P. K. (1999). Apert syndrome: A case report with discussion of craniofacial features. Quintessence International, 30(6), 423-426.