Podocytopathy and Glomerular Basement Membrane Anomalies in Two Patients With Cubilin Gene Mutations

Proteinuria is a frequent finding in pediatric patients and in most cases, it is intermittent or transient. When proteinuria is moderate/severe and persistent, it may require an extensive complementary study, histopathological examination and genetic test, in order to clarify its etiology. Cubilin (...

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Detalles Bibliográficos
Autores principales: Madureira Gomes, Sara, Igreja, Ana Isabel, Silva, Roberto, Oliveira, João Paulo, Pinto, Helena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9998106/
https://www.ncbi.nlm.nih.gov/pubmed/36913226
http://dx.doi.org/10.7759/cureus.34730

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9998106/
https://www.ncbi.nlm.nih.gov/pubmed/36913226
http://dx.doi.org/10.7759/cureus.34730

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