Gobeil F, Labbé A C, LePage S
Department of Medicine, Division of Cardiology, Centre hospitalier universitaire de Sherbrooke, Québec, Canada.
Can J Cardiol. 1996 Mar;12(3):297-9.
Congenital complete atrioventricular block is quite rare, with usually a benign clinical evolution. However, because the first manifestation can be sudden death, it is important to evaluate patients and to establish clear prognostic criteria. A case of complete congenital atrioventricular block in a 38-year-old woman is presented to illustrate these criteria.
先天性完全性房室传导阻滞相当罕见,通常临床进展良性。然而,由于首发表现可能是猝死,因此评估患者并建立明确的预后标准很重要。本文介绍了一名38岁女性的完全性先天性房室传导阻滞病例,以阐明这些标准。