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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 (...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Cureus
2023
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| Materias: | |
| 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 |