Axenfeld-Rieger Syndrome: Rare Case Presentation and Overview

被引:3
|
作者
Agarwal, Padmanidhi [1 ]
Jain, Kanav [1 ]
Sandesh, Shubham [2 ]
Chopra, Sakshi [3 ]
机构
[1] AIIMS, Dept Dent & Maxillofacial Surg, Rishikesh, India
[2] Teerthanker Mahaveer Dent Coll, Moradabad, India
[3] King Georges Med Univ, Dept Prosthodont, Lucknow, Uttar Pradesh, India
来源
关键词
Axenfeld-Rieger syndrome; Anodontia; Craniofacial abnormalities; Oligodontia; Telecanthus; Tooth abnormalities; MUTATIONS; SPECTRUM; PITX2;
D O I
10.1007/s12663-019-01307-9
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Axenfeld-Rieger syndrome (ARS) is an extremely rare autosomal dominant disorder characterized by ocular, craniofacial, dental and periumbilical abnormalities. We present a case of a 10-year-old boy. Its awareness among oral surgeons is essential for timely diagnosis and subsequent prevention of ophthalmic and systemic complications as craniofacial and dental features constitute the early recognizable symptoms of this syndrome. Systematic ophthalmic surgeries aid in relieving vision abnormalities, while symptomatic dental treatment should be provided for masticatory and esthetic rehabilitation.
引用
收藏
页码:364 / 369
页数:6
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