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Hyponatremia - A rare complication of Gitelman's syndrome
Gitelman's syndrome (GS) is a rare autosomal recessive disorder caused by mutations in thiazide-sensitive NaCl cotransporter. We report a 49-year-old, normotensive lady with prolonged hypokalemia since her 20s who was diagnosed with GS at our renal clinic. During follow-up, she was found to hav...
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| Publicat a: | Indian J Nephrol |
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| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Medknow Publications & Media Pvt Ltd
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5255997/ https://ncbi.nlm.nih.gov/pubmed/28182047 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0971-4065.177208 |
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