Woldetensaye Anania G, Runyan Christopher Michael, Koerner Jagger C
Department of Ophthalmology, Wake Forest University School of Medicine, Winston Salem, North Carolina.
Department of Plastic Surgery, Wake Forest University School of Medicine, Winston-Salem, North Carolina.
J AAPOS. 2022 Dec;26(6):338-340. doi: 10.1016/j.jaapos.2022.08.262. Epub 2022 Sep 22.
Waardenburg syndrome (WS) is a congenital developmental disorder characterized by congenital sensorineural hearing loss and pigmentary deficiencies in the iris, hair, and skin. Ocular associations of WS include choroidal and iris hypopigmentation and foveal hypoplasia. Possible associations include cataracts and retinal vein occlusion. We report the first case of neurotrophic cornea and relate our experience with neurotization surgery.
瓦登伯革氏综合征（WS）是一种先天性发育障碍，其特征为先天性感音神经性听力损失以及虹膜、毛发和皮肤色素沉着不足。WS的眼部相关表现包括脉络膜和虹膜色素减退以及黄斑发育不全。可能的相关表现包括白内障和视网膜静脉阻塞。我们报告了第一例神经营养性角膜病例，并分享了我们在神经化手术方面的经验。
