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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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| Publicado en: | BMJ Case Rep |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
BMJ Publishing Group
2016
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| Assuntos: | |
| Acceso en liña: | 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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