A delayed diagnosis of catecholaminergic polymorphic ventricular tachycardia with a mutant of RYR2 at c.7580T>G for 6 years in a 9-year-old child

RATIONALE: Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a rare but potentially lethal inherited arrhythmia syndrome induced by adrenergic stress. Due to the atypical clinical manifestations in early age, limited recognition and experience of pediatric cardiologists, and low awaren...

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Detalles Bibliográficos
Autores principales: Duan, Hongyu, Lu, Yongyi, Yan, Song, Qiao, Lina, Hua, Yimin, Li, Yifei, Zhou, Kaiyu, Wang, Chuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2018
Materias:
6200
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5916663/
https://www.ncbi.nlm.nih.gov/pubmed/29668588
http://dx.doi.org/10.1097/MD.0000000000010368

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5916663/
https://www.ncbi.nlm.nih.gov/pubmed/29668588
http://dx.doi.org/10.1097/MD.0000000000010368

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