Bilateral anterior lenticonus in a young patient with Alport and #8217;s syndrome

A. Aksoy, I. Yaşar, M. Aslankurt, L. Aslan, O. Oğuzhan
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引用次数: 1

Abstract

Alport's syndrome is a familial disease affecting basement membrane collagen and characterized by progressive kidney disfunction, hearing disorder and ocular abnormalities. Twenty four years old man presented with visual impairment in our outpatients clinic. Bilateral anterior lenticonus were seen in ocular slit lamp examination. After clinical examinations, audiological tests and nephrological evaluation, the case was diagnosed as Alport's syndrome. Although males and females are affected equally in this disease, males have poorer prognosis than females owing to renal failure. It is intended to remind this uncommon disease and create awareness for ophthalmologists in the present article.
一例年轻Alport和#8217;s综合征患者的双侧前晶状体
Alport综合征是一种影响基底膜胶原蛋白的家族性疾病,以进行性肾功能障碍、听力障碍和眼部异常为特征。24岁男性,因视力障碍来门诊就诊。眼裂隙灯检查可见双侧前晶状体。经临床检查、听力学检查及肾脏学评估,诊断为Alport综合征。虽然男性和女性在这种疾病中同样受影响,但由于肾功能衰竭,男性的预后比女性差。它的目的是提醒这种罕见的疾病和创造认识眼科医生在这篇文章。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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