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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...
Gorde:
| Argitaratua izan da: | Cureus |
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| Egile Nagusiak: | , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Cureus
2019
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| Gaiak: | |
| Sarrera elektronikoa: | 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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