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Primary Molecular Disorders and Secondary Biological Adaptations in Bartter Syndrome
Bartter syndrome is a hereditary disorder that has been characterized by the association of hypokalemia, alkalosis, and the hypertrophy of the juxtaglomerular complex with secondary hyperaldosteronism and normal blood pressure. By contrast, the genetic causes of Bartter syndrome primarily affect mol...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
SAGE-Hindawi Access to Research
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3177086/ https://ncbi.nlm.nih.gov/pubmed/21941653 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4061/2011/396209 |
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