Ocular colobomata

被引：157

作者：

Onwochei, BC

Simon, JW

Bateman, JB

Couture, KC

Mir, E

机构：

[1] Albany Med Coll, Dept Ophthalmol, Lions Eye Inst, Albany, NY 12208 USA

[2] St Clares Hosp, Dept Family Practice, Schenectady, NY USA

[3] Schenectady Family Hlth Serv, Dept Family Practice, Schenectady, NY USA

[4] Univ Colorado, Dept Ophthalmol, Denver, CO 80202 USA

来源：

SURVEY OF OPHTHALMOLOGY | 2000年 / 45卷 / 03期

关键词：

embryogenesis; genetic disorders; microphthalmia; ocular coloboma; ocular colobomata;

D O I：

10.1016/S0039-6257(00)00151-X

中图分类号：

R77 [眼科学];

学科分类号：

100212 ;

摘要：

Ocular colobomata present diagnostic and therapeutic challenges in patients of all ages, but especially in young children. The "typical" coloboma, caused by defective closure of the fetal fissure, is located in the inferonasal quadrant, and it may affect any Dart of the globe traversed by the fissure from the iris to the optic nerve. Ocular colobomata are often associated with microphthalmia, and they may be idiopathic or associated with various syndromes. Types and severity of complications vary depending on the location and size of the colobomata. This article reviews the pathogeneses, categorization, genetic bases, differential diagnoses and management of ocular coloboma. (Surv Ophthalmol 45: 175-194, 2000. (C) 2000 Elsevier Science Inc. All rights reserved.).

引用

页码：175 / 194

页数：20

共 281 条

[51] FINE MAPPING OF THE LOCUS FOR NEVOID BASAL-CELL CARCINOMA SYNDROME ON CHROMOSOME 9Q [J].