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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Veröffentlicht in:Pediatr Nephrol
Hauptverfasser: 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.
Format: Artigo
Sprache:Inglês
Veröffentlicht: 2019
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Article
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6736764/
https://ncbi.nlm.nih.gov/pubmed/30852663
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00467-019-04210-0
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