Suppr超能文献

乔布综合征中的类科茨病视网膜病变。

Coats-like retinopathy in Joubert syndrome.

作者信息

Abouammoh Marwan A, Al-Shibani Salwa K, Alhawwas Abdulrahman, Bosley Thomas M

机构信息

Ophthalmology Department, College of Medicine, King Saud University, Riyadh, Saudi Arabia.

Ophthalmology Department, College of Medicine, King Saud University, Riyadh, Saudi Arabia.

出版信息

J AAPOS. 2016 Aug;20(4):372-4. doi: 10.1016/j.jaapos.2016.03.018. Epub 2016 Jul 1.

Abstract

An 11-year-old girl with Joubert syndrome was evaluated for a dim red reflex in her left eye. Fundus examination revealed retinal telangiectasias bilaterally compatible with Coats-like pigmentary retinopathy, a phenomenon not previously reported in Joubert syndrome. Coats-like exudative retinopathy may result in permanent visual loss if left untreated. The exudative retinopathy was controlled after multiple sessions of indirect laser photocoagulation and cryotherapy, with a good visual outcome.

摘要

一名患有乔伯特综合征的11岁女孩因左眼暗红色反射接受评估。眼底检查发现双侧视网膜毛细血管扩张,与类科茨色素性视网膜病变相符,这一现象此前在乔伯特综合征中未曾报道。类科茨渗出性视网膜病变若不治疗可能导致永久性视力丧失。经过多次间接激光光凝和冷冻治疗后,渗出性视网膜病变得到控制,视力预后良好。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验