Refractory nephrotic syndrome in focal and segmental glomerulosclerosis by pmm2 genetic variant

datacite.rightshttp://purl.org/coar/access_right/c_abf2
dc.contributor.authorDulce M., Jaime Arturo
dc.contributor.authorConde, Juan
dc.contributor.authorAroca, Gustavo
dc.date.accessioned2025-02-07T21:12:08Z
dc.date.available2025-02-07T21:12:08Z
dc.date.issued2025
dc.description.abstractIntroduction: Nephrotic syndrome (NS) is a clinical condition charac terized by massive proteinuria, edema, hypoalbuminemia, and hyper lipidemia. The etiology may be secondary to systemic, metabolic, infectious, neoplastic, and pharmacological diseases. There is a group of primary causes of unknown etiology whose pathophysiological mech anism is immunological whose most frequent histological pattern in adults is focal segmental glomerulosclerosis (FSGS), minimal change disease and membranous nephropathy that represent podocithopathies. Currently, the KDIGO guidelines add that FSGS may have a genetic etiology, which merits a different diagnostic and therapeutic approach due to its refractoriness to immunosuppressive management, deter mining the causative gene is of great importance to predict its relapse in transplantation. A diversity of genes contributing to podocitopathies (NEPH1, TRPC6, CRB2, FAT1) located in the diaphragm slit has been highlighted, but very few cases have been reported with the PMM2 genetic variant.eng
dc.format.mimetypepdf
dc.identifier.citationWCN25-63 Refractory Nephrotic Syndrome in Focal and Segmental Glomerulosclerosis by PMM2 Genetic Variant Dulce M, Jaime Arturo et al. Kidney International Reports, Volume 10, Issue 2, S565 - S566eng
dc.identifier.issn24680249
dc.identifier.urihttps://hdl.handle.net/20.500.12442/16244
dc.identifier.urlhttps://www.kireports.org/article/S2468-0249(24)03033-X/fulltext
dc.language.isoeng
dc.publisherInternational Society of Nephrology (ISN)spa
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 United Stateseng
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/us/
dc.sourceKidney International Reportseng
dc.sourceVol. 10 No. 2 (Suplemento), (2025)spa
dc.titleRefractory nephrotic syndrome in focal and segmental glomerulosclerosis by pmm2 genetic varianteng
dc.type.driverinfo:eu-repo/semantics/article
dc.type.spaArtículo científico
oaire.versioninfo:eu-repo/semantics/publishedVersion

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