家族性心房快速颤动与 SCN5A 和 KCNQ1 的双重突变相关。
Familial atrial rapid fibrillation associated with double mutations of SCN5A and KCNQ1.
机构信息
Department of Cardiology, Tokyo Women's Medical University, 8-1 Kawada-cho, Shinjuku-ku, Tokyo, Japan.
Department of Pediatric Cardiology, Tokyo Women's Medical University, 8-1 Kawada-cho, Shinjuku-ku, Tokyo, Japan.
出版信息
Cardiol Young. 2021 Aug;31(8):1356-1358. doi: 10.1017/S1047951121000615. Epub 2021 Feb 26.
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.
家族性心房颤动是遗传性的，在儿科人群中偶有发生。通常，颤动的小波频率约为 6 Hz。在此，我们报告了一个家族性病例，其表现为与 KCNQ1 和 SCN5A 突变相关的频率约为 12 至 30 Hz 的快速颤动小波。
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