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Bartter syndrome with long-term follow-up: a case report
Bartter syndrome is a rare inherited disease caused by CLCNKB mutation, which results in inactivation of the chloride channel Kb protein. Bartter syndrome is characterized by extreme hypokalemia, hypochloremia, metabolic alkalosis, hyperrenin-induced angiotensinemia, hyperaldosteronemia, and normal...
Guardado en:
| Publicado en: | J Int Med Res |
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| Autores principales: | , , , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
SAGE Publications
2020
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7705384/ https://ncbi.nlm.nih.gov/pubmed/32857947 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/0300060520947876 |
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