阿尔波特综合征
蛋白尿
肾小球基底膜
医学
肾小球肾炎
疾病
病理
肾小球硬化
皮肤病科
内科学
肾
作者
Shujun Pan,Rizhen Yu,Shikai Liang
标识
DOI:10.3389/fgene.2023.1216809
摘要
Alport syndrome (#308940) is an X-linked genetic disease with clinical manifestations, such as hematuria, proteinuria, renal insufficiency, and end-stage renal disease. The disease is characterized by the thinning of the glomerular basement membrane in the early stages and the thickening of the glomerular basement membrane in the late stages and may be associated with ocular lesions and varying degrees of sensorineural deafness. Herein, we report a case of Alport syndrome caused by a de novo mutation in COL4A5 . The patient was a young male with clinical manifestations of hematuria and massive proteinuria who was diagnosed with Alport syndrome based on renal pathology and genetic testing.
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