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Rare combination in an infant patient: trisomy 7p and tetralogy of fallot
Cardiology in the Young ( IF 1 ) Pub Date : 2022-09-06 , DOI: 10.1017/s1047951122002062
Osman Guvenc 1 , Murat Saygi 1 , Tugba Akin Duman 2
Affiliation  

This case report presents an infant patient with the association of trisomy 7p and tetralogy of fallot (TEF). Patients diagnosed with trisomy 7p should certainly be scheduled for an echocardiographic exam and be scanned for any CHDs that may accompany it. The CHDs that most frequently accompany this syndrome include atrial septal defect, ventricular septal defect, and patent ductus arteriosis. Yet, it should be known that TEF may also be present, albeit rarely.



中文翻译:

婴儿患者的罕见组合:7p 三体和法洛四联症

本病例报告介绍了一名患有 7p 三体和法洛四联症 (TEF) 相关的婴儿患者。诊断为 7p 三体的患者当然应该安排进行超声心动图检查,并扫描任何可能伴随的 CHD。最常伴随该综合征的冠心病包括房间隔缺损、室间隔缺损和动脉导管未闭。然而,应该知道 TEF 也可能存在,尽管很少。

更新日期:2022-09-06
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