Apert syndrome: A case report with discussion of craniofacial features

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

Apert syndrome: A case report with discussion of craniofacial features

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

^*Corresponding author for this work

Manipal College of Dental Sciences, Manipal

Research output: Contribution to journal › Article › peer-review

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 language	English
Pages (from-to)	423-426
Number of pages	4
Journal	Quintessence International
Volume	30
Issue number	6
Publication status	Published - 01-06-1999

All Science Journal Classification (ASJC) codes

General Dentistry

Cite this

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title = "Apert syndrome: A case report with discussion of craniofacial features",

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.",

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AU - Ahsan, Auswaf

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AU - Pai, Keerthilatha M.

AU - Dayal, Promod K.

PY - 1999/6/1

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N2 - 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.

AB - 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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Apert syndrome: A case report with discussion of craniofacial features

Abstract

All Science Journal Classification (ASJC) codes

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