Tiwari Uma Sharan, Aishwarya Ankita, Kujur Rashmi
Department of Ophthalmology, Gajra Raja Medical College, Gwalior, India.
Rom J Ophthalmol. 2018 Jul-Sep;62(3):228-230.
Alport's syndrome is an inherited disease characterized by hearing loss, progressive renal failure and ocular abnormalities like anterior lenticonus, corneal opacities, cataract, fleck retinopathies, and temporal retinal thinning. To have anterior and posterior lenticonus in the same eye in this syndrome is a rare finding and only a few such reports are available. Hereby, we report a case of a 22-year-old male with bilateral combined anterior and posterior lenticonus with sensorineural deafness and nephritis leading to the diagnosis of Alport's syndrome.
奥尔波特综合征是一种遗传性疾病，其特征为听力丧失、进行性肾衰竭以及眼部异常，如前圆锥形晶状体、角膜混浊、白内障、斑点状视网膜病变和颞侧视网膜变薄。在该综合征中，同一只眼睛出现前、后圆锥形晶状体是一种罕见的发现，仅有少数此类报告。在此，我们报告一例22岁男性病例，其双眼合并前、后圆锥形晶状体，并伴有感音神经性耳聋和肾炎，最终诊断为奥尔波特综合征。
