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肥厚型心肌病作为先天性巨细胞病毒感染的临床组成部分。

Hypertrophic Cardiomyopathy as a Clinical Component of Congenital Cytomegalovirus Infection.

作者信息

Demir F, Yilmazer M M, Dalli S, Yolbaş I, Uluca U, Bilici M, Turan M I

机构信息

Department of Pediatric Cardiology, Faculty of Medicine, Dicle University, Diyarbakır, Turkey.

Department of Pediatric Cardiology, Behçet Uz Children's Hospital, Izmir, Turkey.

出版信息

West Indian Med J. 2015 May 11;65(2):409-411. doi: 10.7727/wimj.2014.276.

Abstract

We report hypertrophic cardiomyopathy in a newborn with congenital cytomegalovirus infection. The neonate had distinct signs of congenital cytomegalovirus infection including petechiae, jaundice, intracranial calcifications, cerebral ventriculomegaly and chorioretinitis together with hypertrophic cardiomyopathy. Following determination of anti-cytomegalovirus IgM, viral DNA was also isolated from the plasma of the patient by polymerase chain reaction. Although cytomegalovirus is a relatively frequent cause of myocarditis in childhood, it was rarely reported to be associated with cardiac abnormalities such as structural heart disease, atrioventricular block, or dilated cardiomyopathy. To our knowledge, this is the first case with congenital cytomegalovirus infection and hypertrophic cardiomyopathy.

摘要

我们报告了一名患有先天性巨细胞病毒感染的新生儿肥厚型心肌病。该新生儿有先天性巨细胞病毒感染的明显体征,包括瘀点、黄疸、颅内钙化、脑室扩大和脉络膜视网膜炎,同时伴有肥厚型心肌病。在测定抗巨细胞病毒IgM后,还通过聚合酶链反应从患者血浆中分离出病毒DNA。虽然巨细胞病毒是儿童心肌炎相对常见的病因,但很少有报道称其与结构性心脏病、房室传导阻滞或扩张型心肌病等心脏异常有关。据我们所知,这是首例先天性巨细胞病毒感染合并肥厚型心肌病的病例。

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