A case of congenital nephrotic syndrome due to <i>ARHGDIA</i> gene mutation

Author:

Goda Satoshi1,Ohta Toshiyuki1,Ohno Norioki2,Tani Hiroo3,Tsuboi Ayana3,Ono Hiroaki3,Jinno Kazuhiko3,Sakakibara Nana4,Nozu Kandai4

Affiliation:

1. Department of Pediatric Nephrology, Hiroshima Prefectural Hospital

2. Department of Pediatrics, Hiroshima City Hiroshima Citizens Hospital

3. Department of Pediatrics, Hiroshima Prefectural Hospital

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

Publisher

Japanese Society for Pediatric Nephrology

Reference13 articles.

1. 1) AbuMaziad AS, Abusaleh R, Bhati S: Congenital nephrotic syndrome. J Perinatol 2021; 41: 2704–2712.

2. 2) 佐藤舞:ギャロウェイ・モワト(Galloway-Mowat)症候群.小児診療 2018; 81: 1769–1772.

3. 3) 濱崎祐子,綾邦彦,濱田陸,村松真樹,松本真輔,釜江智佳子:難治性疾患政策研究事業「小児腎領域の希少・難治性疾患群の診療・研究体制の発展」(厚生労働科学研究費補助金)作成 フィンランド型先天性ネフローゼ症候群診療の手引き.東京,大西印刷社,2022.

4. 4) Leffers H, Nielsen MS, Andersen AH, Honore B, Madsen P, Vandekerckhove J, Celis JE: Identification of two human rho GDP dissociation inhibitor proteins whose overexpression leads to disruption of the actin cytoskeleton. Exp Cell Res 1993; 209: 165–174.

5. 5) Xie F, Shao S, Aziz AUR, Zhang B, Wang H, Liu B: Role of rho-specific guanine nucleotide dissociation inhibitor alfa regulation in cell migration. Acta Histochem 2017; 119: 183–189.

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