Prevalence of low molecular weight proteinuria and Dent disease 1 CLCN5 mutations in proteinuric cohorts.

Background: Dent disease type 1 (DD1) is a rare X-linked disorder caused mainly by CLCN5 mutations. Patients may present with nephrotic-range proteinuria leading to erroneous diagnosis of focal segmental glomerulosclerosis (FSGS) and unnecessary immunosuppressive treatments. Methods: The following c...

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Publicado en:	Pediatric Nephrology Vol. 35; no. 4; pp. 633 - 641
Autores principales:	Beara-Lasic, Lada, Cogal, Andrea, Mara, Kristin, Enders, Felicity, Mehta, Ramila A., Haskic, Zejfa, Furth, Susan L., Trachtman, Howard, Scheinman, Steven J., Milliner, Dawn S., Goldfarb, David S., Harris, Peter C., Lieske, John C.
Formato:	research tables/charts Journal Article
Publicado:	Springer Nature Apr2020
Acceso en línea:	Ver este registro en EBSCOhost