A Case Series of 4 Patients with Congenital Nephrotic Syndrome

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Çocuk Dergisi
Volume:23 Issue:1
A Case Series of 4 Patients with Congenital Nephrotic Syndrome

A Case Series of 4 Patients with Congenital Nephrotic Syndrome

Authors : Zehra AYDIN, Mihriban İNÖZÜ, İbrahim ŞAHİN, Umut Selda BAYRAKÇI

Pages : 101-104

Doi:10.26650/jchild.2023.1000965

View : 20 | Download : 12

Publication Date : 2023-03-27

Article Type : Other Papers

Abstract :Congenital nephrotic syndrome insert ignore into journalissuearticles values(CNS); is a rare hereditary kidney disease that begins at birth or within the first three months of life. CNS is characterized by severe proteinuria, hypoalbuminemia, edema, and hyperlipidemia. It is primarily caused by gene mutations that result in damage to the glomerular filtration barrier. We wanted to present the clinical course of our four patients, one of whom was in spontaneous remission. In this study, we wanted to draw attention to the different clinical courses of patients with nephrin mutations.
Keywords : Çocuk, Konjenital Nefrotik Sendrom, Nefrin

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