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一名7号染色体长臂缺失患者的先天性心脏缺陷

Congenital heart defect in a patient with deletion of chromosome 7q.

作者信息

Tiller G E, Watson M S, Duncan L M, Dowton S B

机构信息

Edward Mallinckrodt Department of Pediatrics, Washington University School of Medicine, St. Louis, MO 63110.

出版信息

Am J Med Genet. 1988 Feb;29(2):283-7. doi: 10.1002/ajmg.1320290206.

Abstract

We describe a premature male infant with a terminal deletion of 7q [del(7) (pter----q34:)]. Manifestations include low birth weight, hypertelorism, bilateral cleft lip and palate, cryptorchidism, and a complex congenital heart defect. The latter consisted of hypoplasia of the main pulmonary artery, absent pulmonary valve, ventricular septal defect, and anomalous right pulmonary artery. We briefly review the spectrum of heart defects seen with chromosome 7 deletions, and comment on the incidence of this unusual heart lesion.

摘要

我们描述了一名患有7号染色体长臂末端缺失[del(7)(pter----q34:)]的早产男婴。临床表现包括低出生体重、眼距过宽、双侧唇腭裂、隐睾以及复杂的先天性心脏缺陷。后者包括主肺动脉发育不全、肺动脉瓣缺如、室间隔缺损和右肺动脉异常。我们简要回顾了与7号染色体缺失相关的心脏缺陷谱,并对这种不寻常心脏病变的发生率进行了评论。

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