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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...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
King Faisal Specialist Hospital and Research Centre
2019
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6926230/ https://www.ncbi.nlm.nih.gov/pubmed/31890843 http://dx.doi.org/10.1016/j.ijpam.2019.06.005 |