COL4A gene variants are common in children with hematuria and a family history of kidney disease
Author:
Publisher
Springer Science and Business Media LLC
Subject
Nephrology,Pediatrics, Perinatology and Child Health
Link
https://link.springer.com/content/pdf/10.1007/s00467-023-05993-z.pdf
Reference26 articles.
1. KDIGO Conference Participants (2022) Genetics in chronic kidney disease: conclusions from a kidney disease: improving global outcomes (KDIGO) controversies conference. Kidney Int 101:1126–1141. https://doi.org/10.1016/j.kint.2022.03.019
2. Bullich G, Domingo-Gallego A, Vargas I et al (2018) A kidney-disease gene panel allows a comprehensive genetic diagnosis of cystic and glomerular inherited kidney diseases. Kidney Int 94:363–371. https://doi.org/10.1016/j.kint.2018.02.027
3. Mrug M, Bloom MS, Seto C et al (2021) Genetic testing for chronic kidney diseases: clinical utility and barriers perceived by Nephrologists. Kidney Med 3:1050–1056. https://doi.org/10.1016/j.xkme.2021.08.006
4. Vehaskari VM, Rapola J, Koskimies O, Savilahti E, Vilska J, Hallman N (1979) Microscopic hematuria in school children: epidemiology and clinicopathologic evaluation. J Pediatr 95:676–684. https://doi.org/10.1016/s0022-3476(79)80710-6
5. Lieberman K, Chang A, Block G et al (2022) The KIDNEYCODE program: diagnostic yield and clinical features of individuals with chronic kidney disease. Kidney360 3:900–909. https://doi.org/10.34067/KID.0004162021
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1. Whole exome sequencing approach for identification of the molecular etiology in pediatric patients with hematuria;Clinica Chimica Acta;2024-02
2. Genomic Approaches for Monogenic Kidney Diseases: A Comparative Review of Diagnostic Methods and Precision Medicine Implications;Applied Sciences;2023-11-27
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