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坎特雷尔五联症:一例报告

Pentalogy of Cantrell: a case report.

作者信息

Jafarian Amir Hossein, Omidi Abbas Ali, Fazel Alireza, Sadeghian Hamed, Joushan Bahareh

机构信息

Department of Pathology, Ghaem Hospital, Mashhad University of Medical Sciences, Mashhad, Iran.

出版信息

J Res Med Sci. 2011 Jan;16(1):105-9.

Abstract

Cantrell's pentalogy (CP), a rare congenital malformation, consists of the supraumbilical abdominal wall defect, the sterna lower part defect and agenesis of the anterior portion of the diaphragm, an absence of the diaphragmatic part of the pericardium, and a malformation of cardia. This case report presents a female neonate, who was born at 32 weeks of conception, weighing 1300 g and was admitted one hour after delivery. She had the five anatomical defects known for Cantrell's Pentalogy. Moreover, autopsy revealed a bilateral cleft lip and palate, a patent ductus arteriosus, and an atrial and ventricular septal defect.

摘要

坎特雷尔五联症(CP)是一种罕见的先天性畸形,包括脐上腹壁缺损、胸骨下部缺损、膈肌前部发育不全、心包膈部缺如以及心脏畸形。本病例报告介绍了一名女性新生儿,其孕32周出生,体重1300克,出生后1小时入院。她具有坎特雷尔五联症所具有的五种解剖学缺陷。此外,尸检发现双侧唇腭裂、动脉导管未闭以及房间隔和室间隔缺损。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bed8/3063425/38948b64ed57/JRMS-16-105-g001.jpg

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