Congenital nephrotic syndrome in a newborn with glycogen storage disease and Wilms tumor 1 (WT1) mutation

CEN Case Reports 2026 Open access

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Authors: Luigi Annicchiarico Petruzzelli, Oriana De Marco, Nicola Improda, Paolo Giannattasio, Ilaria Luongo, Martina Carucci, Barbara Brunetti, Vittorio Serio, Bruno Minale, Gabriele Malgieri
DOI: 10.1007/s13730-025-01067-1
Cited by: 0
References: 46

Fields of Study & Subjects

Glycogen Storage Diseases and Myoclonus Ion Transport and Channel Regulation Renal Diseases and Glomerulopathies

Publication details

Journal / source
CEN Case Reports
Volume
15
Issue
1
Pages
14–14
Publication date
7 January 2026
Language
EN