Phenotypic variability in a series of four pediatric patients with Andersen-Tawil syndrome: A Saudi experience

Andersen-Tawil syndrome (ATS) is a rare genetic disorder characterized by periodic paralysis, ventricular arrhythmia, and dysmorphic features. However, the classical features are not always seen in the syndrome; therefore, the diagnosis can be challenging. We describe our experience with ATS in Riya...

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Bibliographic Details
Main Authors: Norah A. Alrashed, Waleed M. Al-Manea, Sahar A. Tulbah, Zuhair N. Al-Hassnan
Format: Article
Language:English
Published: Elsevier 2019-12-01
Series:International Journal of Pediatrics and Adolescent Medicine
Online Access:http://www.sciencedirect.com/science/article/pii/S2352646718301984

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