Familial atrial rapid fibrillation associated with double mutations of SCN5A and KCNQ1

Autor:	Morio Shoda, Keiko Toyohara, Miwa Kanai
Rok vydání:	2021
Předmět:	medicine.medical_specialty Scn5a gene macromolecular substances 030204 cardiovascular system & hematology NAV1.5 Voltage-Gated Sodium Channel 03 medical and health sciences Familial case 0302 clinical medicine Internal medicine Atrial Fibrillation medicine Humans Child Fibrillation business.industry General Medicine medicine.disease 030228 respiratory system KCNQ1 Potassium Channel Mutation Pediatrics Perinatology and Child Health Cardiology medicine.symptom Cardiology and Cardiovascular Medicine business Familial atrial fibrillation Paediatric population
Zdroj:	Cardiology in the Young. 31:1356-1358
ISSN:	1467-1107 1047-9511
Popis:	Familial atrial fibrillation is inherited and sporadically occurs in the paediatric population. Generally, fibrillated wavelets are reported at a frequency of approximately 6 Hz. Herein, we report a familial case presenting rapidly fibrillated wavelets at frequencies of approximately 12 to 30 Hz associated with KCNQ1 and SCN5A mutations.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fa7c0c74e639e5f180a01a55b646b4d https://doi.org/10.1017/s1047951121000615 Zobrazit plný text záznamu