A novel EMD mutation in a Chinese family with initial diagnosis of conduction cardiomyopathy. Issue 1 (3rd December 2018)

• Record Type: Journal Article
• Authors: Zhou, Junfeng; Li, Hui; Li, Xiangping; Li, Yonggui; Yang, Mei; Shi, Gaoxing; Xu, Danyan; Shi, Xiaoliu
• Is Part Of: Brain and behavior. Volume 9:Issue 1(2019)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2018-12-03
• Subjects: conduction cardiomyopathy -- EMD gene -- novel mutation -- predominant cardiac phenotype -- X‐linked Emery–Dreifuss muscular dystrophy; Neurology -- Periodicals; Neurosciences -- Periodicals; Psychology -- Periodicals; Psychiatry -- Periodicals; 616.8005
• DOI: 10.1002/brb3.1167
• Languages: English
• ISSNs: 2162-3279

Abstract

Abstract: Introduction: Emery–Dreifuss muscular dystrophy (EDMD) is a hereditary myopathy characterized as triad of muscular dystrophy, joint contractures, and conduction cardiomyopathy. In this study, we diagnosed a X‐linked recessive EDMD patient with severe conduction cardiomyopathy while noteless muscular and joint disorders. Methods: A Chinese cardiomyopathy family spanning four generations was enrolled in the study. Targeted next‐generation sequencing (NGS) was performed to identify the underlying mutation in the proband and validated by Sanger sequencing. Segregation analysis was applied to all 13 participants. Results: A novel frameshift mutation (c.253_254insT, p.Y85Lfs*8) of emerin gene ( EMD ) was found and co‐segregated with family members. Other than the typical manifestations of X‐linked EDMD, this patient presented inconspicuous muscular disorders which were later diagnosed after the mutation been identified. Conclusions: This study enriches the EMD gene mutation database and reminds us of the possibility of EDMD while encountering patients with severe heart rhythm defects or dilated cardiomyopathy of unknown etiology, even if they have neither obvious skeletal muscle disorder nor joint involvement. Abstract : X‐linked Emery–Dreifuss muscular dystrophy is a hereditary myopathy. A Chinese family with initial diagnosis of conduction cardiomyopathy. A novel frameshift mutation (c.253_254insT, p.Y85Lfs*8) of emerin gene(EMD).