Lacrimal drainage anomalies in Rubinstein-Taybi syndrome: case report and review of literature

被引：5
|
作者：
Naik, Jaee Milind [1 ]
Naik, Milind N. [2 ]
Ali, Mohammad Javed [2 ]
机构：
[1] St Johns Med Coll, Dept Anat, Bengaluru, India
[2] LV Prasad Eye Inst, Govindram Seksaria Inst Dacryol, Hyderabad, India
来源：
ORBIT-THE INTERNATIONAL JOURNAL ON ORBITAL DISORDERS-OCULOPLASTIC AND LACRIMAL SURGERY | 2019年 / 38卷 / 04期
关键词：
Rubinstein-Taybi syndrome; lacrimal; CNLDO; nasolacrimal duct; ocular;
D O I：
10.1080/01676830.2018.1515961
中图分类号：
R77 [眼科学];
学科分类号：
100212 ;
摘要：
Rubinstein-Taybi syndrome is a rare multisystem disorder characterized by broad thumbs and first toes, short stature, microcephaly, delayed milestones, beak nose, and hypertelorism. Lacrimal drainage anomalies are not uncommon in this syndrome. We present a patient with Rubinstein-Taybi syndrome with bilateral congenital nasolacrimal duct obstruction and left-sided grossly dilated nasolacrimal duct.
引用
收藏
页码：335 / 337
页数：3
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