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莱伯遗传性视神经病变与肥厚型心肌病。

Leber's Hereditary Optic Neuropathy and Hypertrophic Cardiomyopathy.

作者信息

Hey Thomas Morris, Nielsen Søren Kristian, Eriksen Ulrik, Hansen Frederikke, Mogensen Jens

机构信息

Department of Cardiology, Lillebaelt Hospital-Vejle, Vejle, Denmark.

Department of Cardiology, Odense University Hospital, Odense, Denmark.

出版信息

CJC Open. 2022 Jun 17;4(9):813-815. doi: 10.1016/j.cjco.2022.06.005. eCollection 2022 Sep.

Abstract

Leber's hereditary optic neuropathy (LHON) is a mitochondrial condition that gradually affects the central vision. In the current case report, we present 2 relatives with LHON due to a pathogenic variant within with a clinical phenotype resembling hypertrophic cardiomyopathy, including a short PQ-interval and hypertrophy on electrocardiogram as well as severe hypertrophy of the left ventricle on echocardiography. These findings highlight the importance of offering routine cardiac investigation to patients with LHON and their relatives carrying the variant to hopefully improve correct diagnosis and clinical management of LHON patients.

摘要

Leber遗传性视神经病变(LHON)是一种线粒体疾病,会逐渐影响中心视力。在本病例报告中,我们介绍了2名患有LHON的亲属,其致病变异体与肥厚型心肌病的临床表型相似,包括心电图上PQ间期缩短和肥厚,以及超声心动图显示左心室严重肥厚。这些发现凸显了对LHON患者及其携带该变异体的亲属进行常规心脏检查的重要性,有望改善LHON患者的正确诊断和临床管理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/669d/9486854/b35ea2b790b6/gr1.jpg

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