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Management of Liddle Syndrome in Pregnancy: A Case Report and Literature Review
Liddle syndrome is an autosomal dominant genetic condition that causes hypertension and hypokalemia due to a gain-of-function mutation in the SCNN1B or SCNN1G genes which code for the epithelial sodium channel in the kidney. This leads to increased sodium and water reabsorption causing hypertension....
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Publicado no: | Case Rep Obstet Gynecol |
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Main Authors: | , , , |
Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
Hindawi
2017
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Assuntos: | |
Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5370477/ https://ncbi.nlm.nih.gov/pubmed/28396810 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2017/6279460 |
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