دورية أكاديمية

Indications for genetic examinations in children with bradyarrhythmias

التفاصيل البيبلوغرافية
العنوان: Indications for genetic examinations in children with bradyarrhythmias
المؤلفون: E. B. Polyakova, N. V. Shcherbakova, M. A. Shkolnikova
المصدر: Rossijskij Vestnik Perinatologii i Pediatrii, Vol 67, Iss 3, Pp 117-121 (2022)
بيانات النشر: Ltd. “The National Academy of Pediatric Science and Innovation”, 2022.
سنة النشر: 2022
المجموعة: LCC:Pediatrics
مصطلحات موضوعية: дети, брадиаритмии, наследственный синдром слабости синусного узла, наследственная атриовентрикулярная блокада, врожденное нарушение проводимости, Pediatrics, RJ1-570
الوصف: The nature of hereditary cardiac conduction diseases can be determined by using genetic testing. However, due to the absence of large studies, as well as the phenotypic variability of the electrocardiographic and clinical manifestations in patients with bradyarrhythmias, and a positive genetic test there are difficulti to evaluate its effectiveness. The article presents indications for genetic examinations in children with bradyarrhythmias, developed in the Children’s Center for Cardiac Arrhythmias and summarizes the recommendations for patients with cardiac conduction disorders.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: Russian
تدمد: 1027-4065
2500-2228
Relation: https://www.ped-perinatology.ru/jour/article/view/1662; https://doaj.org/toc/1027-4065; https://doaj.org/toc/2500-2228
DOI: 10.21508/1027-4065-2022-67-3-117-121
URL الوصول: https://doaj.org/article/afbac6024d3146849e5419b180e0c73d
رقم الأكسشن: edsdoj.fbac6024d3146849e5419b180e0c73d
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:10274065
25002228
DOI:10.21508/1027-4065-2022-67-3-117-121