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

Internet

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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