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Acquired Gitelman Syndrome Associated with Systemic Sclerosis
Gitelman syndrome is an inherited renal disorder characterized by hypomagnesemia, hypokalemia, hypocalciuria and metabolic alkalosis linked to the genes encoding the thiazide sensitive NaCl cotransporter (NCCT) located on the distal convoluted tubule of the kidney. It usually presents in late childh...
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| Yayımlandı: | Cureus |
|---|---|
| Asıl Yazarlar: | , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Cureus
2019
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6430306/ https://ncbi.nlm.nih.gov/pubmed/30931194 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7759/cureus.3923 |
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