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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...
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| Publicado no: | Int J Pediatr Adolesc Med |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
King Faisal Specialist Hospital and Research Centre
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6926230/ https://ncbi.nlm.nih.gov/pubmed/31890843 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ijpam.2019.06.005 |
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