Onwochei B C, Simon J W, Bateman J B, Couture K C, Mir E
Family Practice Departments of Schenectady Family Health Services and St. Clare's Hospital, Schenectady, NY, USA.
Surv Ophthalmol. 2000 Nov-Dec;45(3):175-94. doi: 10.1016/s0039-6257(00)00151-x.
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 part 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.
眼裂缺损在各年龄段患者中都带来诊断和治疗挑战,尤其是在幼儿中。由胎儿裂闭合缺陷引起的“典型”裂缺损位于鼻下象限,它可能影响从虹膜到视神经的裂所穿过的眼球任何部分。眼裂缺损常与小眼症相关,可能是特发性的,也可能与各种综合征有关。并发症的类型和严重程度因裂缺损的位置和大小而异。本文综述了眼裂缺损的发病机制、分类、遗传基础、鉴别诊断和管理。