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2名兄弟姐妹患有发育不全的肺动脉和主动脉并伴有梗阻性尿路病。

Hypoplastic pulmonary arteries and aorta with obstructive uropathy in 2 siblings.

作者信息

Kashani I A, Strom C M, Utley J E, Marin-Garcia J, Higgins C B

出版信息

Angiology. 1984 Apr;35(4):252-6. doi: 10.1177/000331978403500408.

Abstract

Two sisters who presented with diffuse hypoplasia of pulmonary arteries, relative hypoplasia of ascending aorta, obstructive uropathy, bilateral ureteral reflux, and hydronephrosis, are described. The subsequent course was characterized by progressive and gradual onset of right heart failure, failure to thrive, chronic malabsorption and systemic hypertension. The syndrome which appears to be transmitted by autosomal recessive inheritance can possibly represent a generalized hypoplasia and growth failure of a part or the entire arterial system. Peripheral pulmonary stenosis can occur as an isolated lesion or in association with other congenital cardiac anomalies, as well as in rubella syndrome and the syndrome of supravalvular aortic stenosis. This communication reports two siblings with a hitherto unreported combination of hypoplastic pulmonary arteries, and aorta with identical genito-urinary tract abnormalities.

摘要

本文描述了两姐妹,她们患有肺动脉弥漫性发育不全、升主动脉相对发育不全、梗阻性尿路病、双侧输尿管反流和肾积水。随后的病程特点为右心衰竭逐渐进展、生长发育迟缓、慢性吸收不良和系统性高血压。该综合征似乎通过常染色体隐性遗传传递,可能代表部分或整个动脉系统的广泛性发育不全和生长衰竭。周围性肺动脉狭窄可作为孤立性病变出现,或与其他先天性心脏异常相关,也可出现在风疹综合征和主动脉瓣上狭窄综合征中。本文报道了两例兄弟姐妹,他们患有肺动脉和主动脉发育不全与相同泌尿生殖道异常的罕见组合。

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