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家族性主动脉瓣上狭窄:一项遗传学研究。

Familial supravalvular aortic stenosis: a genetic study.

作者信息

Chiarella F, Bricarelli F D, Lupi G, Bellotti P, Domenicucci S, Vecchio C

机构信息

Division of Cardiology, EO Ospedali Galliera, Genoa, Italy.

出版信息

J Med Genet. 1989 Feb;26(2):86-92. doi: 10.1136/jmg.26.2.86.

Abstract

Supravalvular aortic stenosis (McKusick 18550) is a rare hereditary condition with autosomal dominant transmission. However, the available data have been limited to small family groups which do not allow the definition of the degree of penetrance of the disease. The present study describes a large family with a high frequency of supravalvular aortic stenosis including five generations and 80 subjects, the largest family group with this disease studied so far. The study was carried out prospectively in 66 subjects (clinical examination, ECG, M mode and two dimensional echocardiography). In 14 subjects available data were examined retrospectively. In 10 patients cardiac catheterisation was performed (prospective study in eight). The disease was present in 36 (45%) of the 80 subjects investigated, on the basis of clinical, echocardiographic, and haemodynamic (when available) criteria. The disease was found to be severe in eight cases (22%), moderate in six cases (17%), mild in 13 (36%), and undefined in eight (22%) patients. In one case (3%), multiple pulmonary stenoses were noted in the absence of supravalvular aortic stenosis. Genetic analysis of these data shows, for the first time, the degree of penetrance of the supravalvular aortic stenosis trait (K = 0.86) and confirms that it is transmitted with incomplete penetrance and variable expressivity.

摘要

瓣上主动脉狭窄(麦库西克18550)是一种罕见的常染色体显性遗传疾病。然而,现有数据仅限于小家族群体,无法确定该疾病的外显程度。本研究描述了一个瓣上主动脉狭窄发病率高的大家族,包括五代人共80名受试者,是迄今为止研究该疾病的最大家族群体。该研究对66名受试者进行了前瞻性研究(临床检查、心电图、M型和二维超声心动图)。对14名受试者的现有数据进行了回顾性检查。对10名患者进行了心导管检查(其中8名进行前瞻性研究)。根据临床、超声心动图和血流动力学(如有)标准,在80名被调查的受试者中,有36名(45%)患有该疾病。发现该疾病在8例(22%)中为重度,6例(17%)中为中度,13例(36%)中为轻度,8例(22%)患者中情况不明。在1例(3%)中,在没有瓣上主动脉狭窄的情况下发现了多处肺动脉狭窄。对这些数据的基因分析首次显示了瓣上主动脉狭窄特征的外显程度(K = 0.86),并证实其遗传具有不完全外显和可变表达性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a93a/1015556/1abbc98e318e/jmedgene00052-0015-a.jpg

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