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先天性及儿童期1型强直性肌营养不良的心脏异常

Cardiac Abnormalities in Congenital and Childhood Myotonic Muscular Dystrophy Type 1.

作者信息

Sharma Anjali, Singh Sandeep, Mishra Shri K

机构信息

Keck School of Medicine, University of Southern California, Los Angeles, California, United States.

College of Osteopathic Medicine of the Pacific, Western University of Health and Sciences, Pomona, California, United States.

出版信息

Neuropediatrics. 2017 Feb;48(1):42-44. doi: 10.1055/s-0036-1597546. Epub 2016 Dec 19.

Abstract

Myotonic dystrophy often presents with cardiac abnormalities, particularly conduction defects, that factor into an increased risk of sudden cardiac death. Myotonic dystrophy has two forms, myotonic dystrophy type 1 (DM1) and DM2, and is a multisystemic disorder that presents in a wide, clinical spectrum and age range. A distinguishing feature of DM1 is the existence of a congenital form. Though research on cardiac involvement has been conducted on patients with the adult form of myotonic dystrophy, there have been few studies focused on cardiac involvement in pediatric patients with congenital myotonic dystrophy type 1 (CDM1). In this study, a survey was conducted to determine the prevalence and variations of cardiac abnormalities in pediatric patients with CDM1. This preliminary study found a prevalence of 25.8% CDM1 pediatric patients with cardiac abnormalities in a sample size of 31 patients.

摘要

强直性肌营养不良常伴有心脏异常,尤其是传导缺陷,这会增加心源性猝死的风险。强直性肌营养不良有两种类型,即强直性肌营养不良1型(DM1)和DM2,是一种多系统疾病,临床表现广泛,发病年龄范围广。DM1的一个显著特征是存在先天性形式。虽然已经对成年型强直性肌营养不良患者的心脏受累情况进行了研究,但很少有研究关注先天性1型强直性肌营养不良(CDM1)儿科患者的心脏受累情况。在本研究中,进行了一项调查以确定CDM1儿科患者心脏异常的患病率和变异性。这项初步研究发现,在31例患者的样本中,25.8%的CDM1儿科患者存在心脏异常。

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