Premature Stroke Secondary to Severe Hypertension Results from Liddle Syndrome Caused by a Novel SCNN1B Mutation

Premature Stroke Secondary to Severe Hypertension Results from Liddle Syndrome Caused by a Novel SCNN1B Mutation

Introduction: Liddle syndrome (LS), an autosomal dominant and inherited monogenic hypertension syndrome caused by pathogenic mutations in the epithelial sodium channel (ENaC) genes SCNN1A, SCNN1B, and SCNN1G. Objective: This study was designed to identify a novel SCNN1B missense mutation in a Chines...

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Bibliographic Details
Main Authors: Peng Fan, Di Zhang, Xiao-Cheng Pan, Kun-Qi  Yang, Qiong-Yu Zhang, Yi-Ting Lu, Ying Zhang, Xue-Ying Liu, Wen-Jun Ma, Hui-Min Zhang, Lei Song, Jun Cai, Ya-Xin Liu, Xian-Liang Zhou
Format: Article
Language:English
Published: Karger Publishers 2020-07-01
Series:Kidney & Blood Pressure Research
Subjects:
liddle syndrome
scnn1b mutation
hypertension
stroke
Online Access:https://www.karger.com/Article/FullText/507580

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https://www.karger.com/Article/FullText/507580

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