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

10 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

Fingerprint

Acrocephalosyndactylia
Uvula
Syndactyly
Craniosynostoses
Palate

All Science Journal Classification (ASJC) codes

  • Dentistry(all)

Cite this

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.
Paravatty, Rajesh P. ; Ahsan, Auswaf ; Sebastian, Bastian T. ; Pai, Keerthilatha M. ; Dayal, Promod K. / Apert syndrome : A case report with discussion of craniofacial features. In: Quintessence International. 1999 ; Vol. 30, No. 6. pp. 423-426.
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Paravatty, RP, Ahsan, A, Sebastian, BT, Pai, KM & Dayal, PK 1999, 'Apert syndrome: A case report with discussion of craniofacial features', Quintessence International, vol. 30, no. 6, pp. 423-426.

Apert syndrome : A case report with discussion of craniofacial features. / Paravatty, Rajesh P.; Ahsan, Auswaf; Sebastian, Bastian T.; Pai, Keerthilatha M.; Dayal, Promod K.

In: Quintessence International, Vol. 30, No. 6, 01.06.1999, p. 423-426.

Research output: Contribution to journalArticle

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Paravatty RP, Ahsan A, Sebastian BT, Pai KM, Dayal PK. Apert syndrome: A case report with discussion of craniofacial features. Quintessence International. 1999 Jun 1;30(6):423-426.