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[Cardiopathies in Di George's syndrome].

作者信息

Normand J, Bozio A, André M, Sassolas F, Lagnier M

机构信息

Hôpital cardiovasculaire et pneumologique Louis-Pradel, BP Lyon-Montchat, France.

出版信息

Pediatrie. 1991;46(3):287-91.

PMID:1649445
Abstract

Based on 11 personal cases a large review of the literature (188 cases), the authors studied the frequency and types of cardiac anomalies in Di George syndrome. A cardiac anomaly was found in 86% of published cases. Interrupted aortic arch (27%), truncus arteriosus (27%) and tetralogy of Fallot (22%) are the most frequent anomalies. Interrupted aortic arch and truncus arteriosus, being rare congenital heart diseases, their discovery in a neonate must lead to a systematic search for Di George syndrome.

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