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A case of Bartter syndrome type I with atypical presentations
Bartter syndrome (BS) is an autosomal recessively inherited rare renal tubular disorder characterized by hypokalemic metabolic alkalosis and hyperreninemic hyperaldosteronism with normal to low blood pressure due to a renal loss of sodium. Genetically, BS is classified into 5 subtypes according to t...
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| 主要な著者: | , , , , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
The Korean Pediatric Society
2010
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| 主題: | |
| オンライン・アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3004498/ https://ncbi.nlm.nih.gov/pubmed/21189980 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3345/kjp.2010.53.8.809 |
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