Batkov E N, Mikhaylova V I
Cheboksary branch of S.N. Fedorov National Medical Research Center "MNTK "Eye Microsurgery", Cheboksary, Russia.
Vestn Oftalmol. 2024;140(3):76-81. doi: 10.17116/oftalma202414003176.
Alport syndrome is a hereditary disease characterized by glomerulopathy, manifested by hematuria and/or proteinuria, progressive decline in renal function, often combined with hearing and vision pathology. This article presents a clinical case of spontaneous opening of the anterior lens capsule in a patient with Alport syndrome, accompanied by uveitis and ophthalmic hypertension, and describes the features of the surgical aid and the postoperative period.
奥尔波特综合征是一种以肾小球病为特征的遗传性疾病,表现为血尿和/或蛋白尿,肾功能进行性下降,常伴有听力和视力病变。本文介绍了一例奥尔波特综合征患者晶状体前囊自发开放并伴有葡萄膜炎和高眼压的临床病例,并描述了手术辅助及术后阶段的特点。