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通过对两个阿尔波特综合征家庭进行基因分析对基于肾活检的诊断进行重新评估。

A Re-evaluation of Renal Biopsy-based Diagnoses Through a Genetic Analysis in Two Families with Alport Syndrome.

作者信息

Higashi Yoshiaki, Koga Kenichi, Hasebe Masako, Fukushima Chiho, Omiya Chiaki, Nishioka Keisuke, Nozu Kandai, Yahata Kensei

机构信息

Department of Nephrology, Osaka Red Cross Hospital, Japan.

Department of Pediatrics, Kobe University Graduate School of Medicine, Japan.

出版信息

Intern Med. 2025 Jul 1;64(13):2014-2018. doi: 10.2169/internalmedicine.4485-24. Epub 2024 Dec 5.

Abstract

Alport syndrome is an inherited disorder characterized by progressive renal failure, sensorineural hearing loss, and ocular involvement due to pathogenic variants of genes encoding type IV collagen. A renal biopsy does not reveal specific findings in the early stages; thus, Alport syndrome may be diagnosed as another glomerular disease. We herein report two families that were previously diagnosed with other glomerular diseases based on renal biopsies and were then accurately diagnosed by genetic testing. An early diagnosis may lead to the avoidance of unnecessary biopsies and treatments, and appropriate management may improve the renal prognosis.

摘要

奥尔波特综合征是一种遗传性疾病,其特征为进行性肾衰竭、感音神经性听力丧失以及由于编码IV型胶原的基因发生致病变异而导致的眼部受累。肾活检在早期阶段不会显示出特异性发现;因此,奥尔波特综合征可能被诊断为其他肾小球疾病。我们在此报告两个家族,他们之前基于肾活检被诊断为其他肾小球疾病,随后通过基因检测得到了准确诊断。早期诊断可能有助于避免不必要的活检和治疗,而适当的管理可能改善肾脏预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b8d/12287572/762603feb1b4/1349-7235-64-13-2014-g001.jpg

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