Temporal macular thinning: a salient sign of Alport syndrome

Sharan Silvarajoo, Wai Yong Zheng, Jamalia Rahmat
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Abstract

Alport syndrome is a hereditary, multisystemic disorder that causes abnormalities of the ear, kidney, and eye. A teenager who was suffering from end-stage renal failure and hearing problems was referred to us suspected of Alport syndrome. He did not have any ocular complaints and wore glasses for myopic astigmatism. His best-corrected visual acuity was 6/7.5 bilaterally. Anterior segment examination was unremarkable. Posterior segment examination showed perimacular dot-andfleck retinopathy with bull’s eye maculopathy. Optical coherence tomography revealed temporal macular thinning. The findings were in keeping with the diagnosis of X-linked Alport syndrome. Ocular findings can help diagnose Alport syndrome. Early detection and treatment can help delay the progression of kidney failure.
颞黄斑变薄:阿尔波特综合征的显著标志
阿尔波特综合征是一种遗传性多系统疾病,会导致耳朵、肾脏和眼睛的异常。一位患有终末期肾衰竭和听力问题的青少年被怀疑患有阿尔波特综合征。他没有眼部疾患,因近视散光戴眼镜。双侧最佳矫正视力为6/7.5。前节检查无明显异常。后段检查显示黄斑周围斑点性视网膜病变伴牛眼黄斑病变。光学相干断层扫描显示颞黄斑变薄。这一发现与x连锁阿尔波特综合征的诊断结果一致。眼部检查可以帮助诊断阿尔波特综合征。早期发现和治疗有助于延缓肾衰竭的进展。
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