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Management of a severe case of Gitelman syndrome with poor response to standard treatment
Gitelman syndrome is an autosomal recessive distal renal tubular disorder caused by defective sodium chloride transporters. Biochemically, it presents with hypokalaemic metabolic alkalosis, hypomagnesaemia and hypocalciuria. It is usually managed with oral potassium supplements and potassium-sparing...
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| Vydáno v: | BMJ Case Rep |
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| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BMJ Publishing Group
2016
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5483581/ https://ncbi.nlm.nih.gov/pubmed/26887881 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2015-212375 |
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