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一个患有心脏手综合征的家族。

A family of Holt-Oram syndrome.

作者信息

Ito M, Misawa T, Fujino M, Ito S, Fukumoto T

出版信息

Jpn Heart J. 1975 Jul;16(4):480-7. doi: 10.1536/ihj.16.480.

Abstract

A family of Holt-Oram syndrome is reported. Twenty of 41 living members in the last 3 generations were examined. The propositus expressed typically the cardinal features of this syndrome: atrial septal defect, patent ductus arteriosus, cardiac arrhythmias and conduction block of various types, and hypoplasia of the left thumb. Two individuals were clinically diagnosed to have atrial septal defect without any upper limb anomaly, and 3 showed upper limb anomaly without any sign of congenital heart disease. Other 5 members showed only minor abnormalities, such as funnel chest or mild right ventricular hypertrophy on ECG and VCG. Some of the skeletal abnormalities observed were hitherto undescribed ones. These include generalized hypoplasia of left hand and downward displacement of right sterno-clavicular joint.

摘要

报道了一个 Holt-Oram 综合征家族。对过去三代中的 41 名在世成员中的 20 人进行了检查。先证者典型地表现出该综合征的主要特征:房间隔缺损、动脉导管未闭、各种类型的心律失常和传导阻滞,以及左拇指发育不全。两名个体临床诊断为房间隔缺损但无任何上肢异常,3 名个体表现为上肢异常但无先天性心脏病迹象。另外 5 名成员仅表现出轻微异常,如漏斗胸或心电图和心向量图显示轻度右心室肥厚。观察到的一些骨骼异常是迄今未描述过的。这些包括左手普遍发育不全和右胸锁关节向下移位。

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