Apert syndrome: A case report with discussion of craniofacial features

被引：0

作者：

Paravatty, RP ^{[1
]}

Ahsan, A

Sebastian, BT

Pai, KM

Dayal, PK

机构：

[1] Coll Dent Surg, Dept Oral Diag Med & Radiol, Manipal, India

[2] Coll Dent Surg, Dept Oral Pathol & Microbiol, Manipal, India

[3] Coll Dent Surg, Dept Oral Diag Med & Radiol, Mangalore, India

来源：

QUINTESSENCE INTERNATIONAL | 1999年 / 30卷 / 06期

关键词：

acrocephalosyndactyly; Apert syndrome; craniosynostosis; syndactyly;

D O I：

暂无

中图分类号：

R78 [口腔科学];

学科分类号：

1003 ;

摘要：

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.

引用

页码：423 / 426

页数：4

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