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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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| Gepubliceerd in: | Turk Pediatri Ars |
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| Hoofdauteurs: | , , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Kare Publishing
2020
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7096570/ https://ncbi.nlm.nih.gov/pubmed/32231453 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5152/TurkPediatriArs.2018.6540 |
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