Department of Ophthalmology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100730, China.
Chin Med Sci J. 2022 Jun 30;37(2):159-163. doi: 10.24920/003956. Epub 2022 May 16.
A 2-year-old girl was diagnosed as Weill-Marchesani syndrome with typical systemic features of short stature, short and stubby hands and feet, language disorders and mental retardation. He developed bilateral angle closure glaucoma, ectopia lentis and suffered visual loss from the ocular features of Weill-Marchesani syndrome. The child was successfully treated by combined CO laser-assisted sclerectomy surgery and trabeculectomy.
一位 2 岁女孩被诊断为马凡氏综合征，具有典型的全身性特征，包括身材矮小、手脚短而粗、语言障碍和智力迟钝。她患有双眼闭角型青光眼、晶状体异位，并因马凡氏综合征的眼部特征而导致视力丧失。通过联合 CO 激光辅助巩膜切除术和小梁切除术，该患儿得到了成功治疗。
