Diagnostic Lacunae and Implications of an Automated Implantable Cardioverter Defibrillator Implantation in a Child with Type 3 Long QT (LQT3) Syndrome

A diagnosis of congenital long QT interval syndrome based on history and electrocardiogram was made in a child in the absence of readily available genetic testing. A genotype 3 (LQT3) was suspected after exclusion of other variants as the child was non-responsive to beta-blocker and sodium channel b...

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Detalles Bibliográficos
Autores principales: Maddali, Madan M, Kandachar, Pranav S, Al-Abri, Ismail A, Al-Yamani, Mohammed I
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9244276/
https://www.ncbi.nlm.nih.gov/pubmed/35417973
http://dx.doi.org/10.4103/aca.aca_13_21

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9244276/
https://www.ncbi.nlm.nih.gov/pubmed/35417973
http://dx.doi.org/10.4103/aca.aca_13_21

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