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三尖瓣闭锁与瓣环发育不全:家族性病例报告

Tricuspid atresia and annular hypoplasia: report of a familial occurrence.

作者信息

Kumar A, Victorica B E, Gessner I H, Alexander J A

机构信息

Division of Pediatric Cardiology, University of Florida College of Medicine, Gainesville.

出版信息

Pediatr Cardiol. 1994 Jul-Aug;15(4):201-3. doi: 10.1007/BF00800676.

Abstract

Occurrence of a similar cardiac malformation in multiple family members has been reported for many lesions. Neither tricuspid atresia nor tricuspid annular hypoplasia and tricuspid atresia has been described in multiple members of the same family. We report two cases of tricuspid atresia and one case of tricuspid annular hypoplasia with an atrial septal defect in siblings. The findings in this family suggest an autosomal recessive pattern of inheritance for abnormal tricuspid valve morphogenesis.

摘要

许多病变都有报道称在多个家庭成员中出现类似的心脏畸形。同一家庭的多个成员中均未描述过三尖瓣闭锁或三尖瓣环发育不全合并三尖瓣闭锁的情况。我们报告了两例三尖瓣闭锁病例和一例同胞中合并房间隔缺损的三尖瓣环发育不全病例。该家族的研究结果提示三尖瓣形态异常的常染色体隐性遗传模式。

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