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本文报告了来自两个家族的4例上肢心血管综合征病例,对其胚胎学和遗传学因素作了扼要的讨论。本综合征是一种常染色体显性遗传性疾病,注意合并的上肢畸形有助于确诊和在同一家族中找出其他患者。在诊疗中应注意可能存在的各种心律失常和外周血管畸形。对患者和家属应提出适当的遗传方面的忠告。
This article reports on 4 cases of upper extremity cardiovascular syndrome from two families and briefly discusses their embryology and genetics. This syndrome is an autosomal dominant genetic disease, attention to the merger of upper limb deformity helps to confirm the diagnosis and find other patients in the same family. In the treatment should pay attention to the various arrhythmias and peripheral vascular malformations that may exist. Patients and their families should be given appropriate genetic counseling.