Fetal bradycardia associated with left ventricle noncompaction diagnosed as HCN4 mutations.

IF 0.9 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS Annals of Pediatric Cardiology Pub Date : 2024-07-01 Epub Date: 2024-11-15 DOI:10.4103/apc.apc_138_24
Kosuke Yonehara
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Abstract

A 35-year-old pregnant woman was referred to our hospital because of fetal bradycardia. Fetal echocardiography revealed a normal fetal heart except for slightly prominent trabeculae in the left ventricle, normal cardiac function, and fetal sinus bradycardia with a heart rate of 100 bpm. Electrocardiography (ECG) after birth revealed sinus bradycardia with a heart rate of 70-80 bpm. Transthoracic echocardiography revealed left ventricular noncompaction localized in the apex with normal cardiac function. A 24-h Holter ECG showed a heart rate range of 62-169 bpm without a pause of more than 2 s. A genome analysis performed during the neonatal period revealed a heterozygous inflame variant p.(Ser672_Asp676del)[chr15:g. 73324203_733242] in HCN4 gene. Fetuses with a heart rate less than the 3rd percentile of the gestational age should be followed and screened for congenital heart disease and cardiomyopathy. In addition, inherited arrhythmia syndrome should be considered.

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胎儿心动过缓与左心室不压实相关,诊断为HCN4突变。
一名35岁孕妇因胎儿心动过缓转诊至我院。胎儿超声心动图显示胎儿心脏正常,左心室小梁略突出,心功能正常,胎儿窦性心动过缓,心率100 bpm。出生后心电图显示窦性心动过缓,心率70-80次/分钟。经胸超声心动图显示左心室不致密定位于心尖,心功能正常。24小时动态心电图显示心率范围为62-169 bpm,没有停顿超过2秒。在新生儿时期进行的基因组分析显示了一个杂合的炎症变异p.(Ser672_Asp676del)[chr15:g]。73324203_733242]在HCN4基因。心率低于胎龄第3百分位数的胎儿应进行随访,筛查先天性心脏病和心肌病。此外,还应考虑遗传性心律失常综合征。
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来源期刊
Annals of Pediatric Cardiology
Annals of Pediatric Cardiology CARDIAC & CARDIOVASCULAR SYSTEMS-
CiteScore
1.40
自引率
14.30%
发文量
51
审稿时长
23 weeks
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