Mili-Boussen I, Ghattas M, Ben Romdhane B, Ouertani A
Service d'ophtalmologie, hôpital Charles-Nicolle, boulevard du 9 avril, 1006 Tunis, Tunisie.
Arch Pediatr. 2000 Dec;7(12):1304-6. doi: 10.1016/s0929-693x(00)00147-0.
Alport's syndrome is a familial disorder characterized by progressive renal failure, sensorineural hearing loss and ocular manifestations.
The authors report a case of a 13-year-old child with Alport's syndrome associated with retinal flecks.
Retinal flecks are the most frequent ocular manifestation in Alport's syndrome and are a considerable help to diagnosis. They are often associated with severe renal failure.
奥尔波特综合征是一种家族性疾病,其特征为进行性肾衰竭、感音神经性听力损失和眼部表现。
作者报告一例13岁患有奥尔波特综合征并伴有视网膜斑点的儿童病例。
视网膜斑点是奥尔波特综合征最常见的眼部表现,对诊断有很大帮助。它们常与严重肾衰竭相关。