Department of Ophthalmology, Hospital Sant Joan de Deu, Passeig Sant Joan de Déu 2, 08950, Esplugues de Llobregat, Barcelona, Spain.
Indian J Ophthalmol. 2023 Apr;71(4):1651-1653. doi: 10.4103/IJO.IJO_3260_22.
Stüve-Wiedemann syndrome is a rare bone dysplasia with dysautonomic manifestations. Most patients die in the neonatal period or during infancy because of the multiple complications they present. The main ophthalmological complications reported are reduced corneal reflex, corneal anesthesia, hypolacrimation, and severely reduced blinking. We are going to present the first tarsoconjunctival flap in a Stüve-Wiedemann patient, the surgery, and the results in a 13-year-old patient that came to our hospital because of severe corneal ulceration.
斯蒂夫-威德曼综合征是一种罕见的骨骼发育不良，伴有自主神经表现。由于患者存在多种并发症，大多数患者在新生儿期或婴儿期死亡。报道的主要眼科并发症包括角膜反射减弱、角膜感觉丧失、少泪和严重眨眼减少。我们将介绍首例斯蒂夫-威德曼综合征患者的眼轮匝肌-结膜瓣手术，以及 13 岁因严重角膜溃疡来我院就诊的患者的手术结果。
