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