A case of Type 1 Dent disease presenting with isolated persistent proteinuria

Dent disease is a rare X-linked recessive tubular disorder, characterized by the triad of low molecular-weight proteinuria, hypercalciuria, nephrocalcinosis and/or nephrolithiasis. It is caused by mutations in the CLCN5 gene or OCRL gene. Thirty to 80% of affected males develop end-stage kidney dise...

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Detalles Bibliográficos
Autores principales: Güngör, Tülin, Eroğlu, Fehime Kara, Yazılıtaş, Fatma, Gür, Gökçe, Çakıcı, Evrim Kargın, Ludwig, Michael, Bülbül, Mehmet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kare Publishing 2020
Materias:
Case Report / Olgu Sunumu
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7096570/
https://www.ncbi.nlm.nih.gov/pubmed/32231453
http://dx.doi.org/10.5152/TurkPediatriArs.2018.6540

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7096570/
https://www.ncbi.nlm.nih.gov/pubmed/32231453
http://dx.doi.org/10.5152/TurkPediatriArs.2018.6540

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