双眼颞侧视网膜脉络膜缺损合并后部胚胎毒素及永存瞳孔膜：一例报告

Double temporal retinochoroidal coloboma with posterior embyotoxon and persistent pupillary membrane: a case report.

作者信息

Dhillon Hennaav Kaur, Narote Kalyani Dashrath, Agarkar Sumita

机构信息

Department of Pediatric Ophthalmology and Strabismus, Sankara Nethralaya, Chennai, Tamil Nadu, India.

出版信息

J AAPOS. 2024 Feb;28(1):103818. doi: 10.1016/j.jaapos.2023.11.018. Epub 2024 Jan 18.

DOI:10.1016/j.jaapos.2023.11.018

PMID:38244914

Abstract

Ocular colobomas are typically located in the inferonasal quadrant and attributable to defective fetal fissure closure. Colobomas can, however, affect any part of the eye, from the eyelid to the optic nerve. We present the case of a 7-year-old girl with two retinochoroidal colobomas in an atypical temporal location, with associated other ocular defects.

摘要

眼裂缺损通常位于鼻下象限，是由胎儿裂闭合缺陷引起的。然而，眼裂缺损可影响眼睛的任何部位，从眼睑到视神经。我们报告一例7岁女孩，患有两个非典型颞侧位置的视网膜脉络膜缺损，并伴有其他眼部缺陷。