WCN25-901 CLINICAL AND GENETIC CHARACTERISTICS CHILDREN WITH PROTEINURIA ASSOCIATED WITH CUBN VARIANTS
Persistent glomerular proteinuria is independent predictor for progression to chronic kidney disease. Mutations in the CUBN gene commonly cause Imerslund-Gräsbeck syndrome, while isolated proteinuria as a result of CUBN variants is rarely reported. The aim of the study was to investigate clinical and genetic characteristics in children with persistent proteinuria, associated with CUBN variants.
Authors
- Larisa Prikhodina (ORCID: https://orcid.org/0000-0002-0702-4932)
- Varvara Obukhova
- Svetlana Papizh (ORCID: https://orcid.org/0000-0001-6459-2795)
- E. S. Stolyarevich
Institutions
- Pirogov Russian National Research Medical University (RU)
- V.I.Shumakov Federal Research Center of Transplantology and Artificial Organs (RU)
Publication Details
- Journal
- Kidney International Reports
- Published
- 2025-01-27
- DOI
- https://doi.org/10.1016/j.ekir.2024.11.648
- Primary Topic
- Genomics and Rare Diseases
- Type
- article
- Field-Weighted Citation Impact
- 0.00