Pediatric Liddle Syndrome Caused by a Novel SCNN1G Variant in a Chinese Family and Characterized by Early-Onset Hypertension

BACKGROUND: Liddle syndrome (LS), an autosomal dominant disorder, is a common monogenic hypertension in pediatrics. In this study, we reported a novel SCNN1G variant in a Chinese family with pediatric LS, and conduct a systematic review of epithelial sodium channel (ENaC)-gene-positive LS cases to c...

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Detalles Bibliográficos
Autores principales: Fan, Peng, Pan, Xiao-Cheng, Zhang, Di, Yang, Kun-Qi, Zhang, Ying, Tian, Tao, Luo, Fang, Ma, Wen-Jun, Liu, Ya-Xin, Wang, Lin-Ping, Zhang, Hui-Min, Song, Lei, Cai, Jun, Zhou, Xian-Liang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Original Contributions
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7368168/
https://www.ncbi.nlm.nih.gov/pubmed/32161960
http://dx.doi.org/10.1093/ajh/hpaa037

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7368168/
https://www.ncbi.nlm.nih.gov/pubmed/32161960
http://dx.doi.org/10.1093/ajh/hpaa037

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