APERT SYNDROME (ACROCEPHALO SYNDACTYLY): A RARE BUT RECOGNIZABLE HUMAN MALFORMATION SYNDROME

被引：0

作者：

Ramu, P. ^{[1
]}

Shankar, R. Bhavani ^{[1
]}

Kumar, A. Deepak ^{[1
]}

机构：

[1] King George Hosp, Andhra Med Coll, Dept Paediat, Visakhapatnam, Andhra Pradesh, India

来源：

JOURNAL OF EVOLUTION OF MEDICAL AND DENTAL SCIENCES-JEMDS | 2015年 / 4卷 / 12期

关键词：

Apert Syndrome; Acrocephalosyndactyly; Craniosynostosis;

D O I：

暂无

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

BACKGROUND: Apert syndrome is a rare autosomal dominant Mendelian disorder characterized by a set of recognizable patterns of human malformations, having paediatric, plastic surgical, Ortholpaedic and Dental implications requiring early recognition & effective management strategies for good Cosmetic and functional out-come.

引用

页码：2072 / 2075

页数：4