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Kidney stones and moderate proteinuria as the rare manifestations of Gitelman syndrome

BACKGROUND: Gitelman syndrome (GS) is an autosomal recessive inherited salt-losing tubulopathy (SLT). Here, we describe, for the first time, a case of GS without Gitelman-like features and with concomitant kidney stones, cysts and diabetic nephropathy (DN). CASE PRESENTATION: We described a male pat...

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Bibliografski detalji
Izdano u:BMC Nephrol
Glavni autori: Chen, Qi, Wang, Xiaoyi, Min, Jingjing, Wang, Lin, Mou, Lijun
Format: Artigo
Jezik:Inglês
Izdano: BioMed Central 2021
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC7791706/
https://ncbi.nlm.nih.gov/pubmed/33413160
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12882-020-02211-y
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