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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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Detalles Bibliográficos
Autores principales:	Awadalla, Michael, Patwardhan, Manasi, Alsamsam, Adham, Imran, Nashat
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Hindawi 2017
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5370477/ https://www.ncbi.nlm.nih.gov/pubmed/28396810 http://dx.doi.org/10.1155/2017/6279460

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