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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...
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| Udgivet i: | J Int Med Res |
|---|---|
| Main Authors: | , , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
SAGE Publications
2020
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| Fag: | |
| Online adgang: | 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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