家族性右心房特发性扩张
Familial idiopathic dilatation of the right atrium
ORPHA:1677疾病
定义 英文原文（暂无中文）
A rare congenital heart malformation of unknown etiology that is characterized by an extremely dilated right atrium, and that is usually asymptomatic and fortuitously discovered by echocardiography or chest radiography, and can be sometimes associated with other anomalies such as atrial arrhythmias (e.g. atrial flutter, atrial fibrillation, supraventricular tachycardia), severe tricuspid regurgitation, or atrial thrombus that could lead to potentially life-threatening thromboembolic complications.
基本事实
- 遗传方式
- 未知
- 发病年龄
- 各年龄段
临床表型 24
极常见 99–80%2
- 房间隔扩张 HP:0011995
- 右心房扩大 HP:0030718
常见 79–30%16
- 心室功能异常 HP:0030872
- 腔静脉形态异常 HP:0005345
- 肝脏血管异常 HP:0006707
- 心律失常 HP:0011675
- 心房纤颤 HP:0005110
- 房室传导阻滞 HP:0001678
- 心脏扩大 HP:0001640
- 完全性心脏传导阻滞伴窄QRS波群 HP:0005178
- 呼吸困难 HP:0002094
- 心脏收缩整期杂音 HP:0031667
- 心脏收缩中期杂音 HP:0031665
- 心悸 HP:0001962
- 左心室射血分数降低 HP:0012664
- 右心室肥厚 HP:0001667
- 晕厥 HP:0001279
- 三尖瓣反流 HP:0005180
偶见 29–5%6
- 颈静脉形态异常 HP:3000042
- 肝脏肿大 HP:0002240
- 阵发性房颤 HP:0004757
- 周围性水肿 HP:0012398
- 胸腔积液 HP:0002202
- 癫痫发作 HP:0001250
外部标识与链接
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本页数据来源
- 疾病定义、同义词、基因、表型、流行病学：Orphanet（CC BY 4.0）
- 中文病名：Orphanet 中文包，冻结于 2020-06-01
- 表型中文标签：HPO 简体中文翻译（CHPO 上游成果）