A case with Emery-Dreifuss muscular dystrophy diagnosed forty-two years after onset and implanted with a cardiac resynchronization therapy defibrillator-Reference-Cited by-同舟云学术

A case with Emery-Dreifuss muscular dystrophy diagnosed forty-two years after onset and implanted with a cardiac resynchronization therapy defibrillator

Published:2014 Issue:6 Volume:54 Page:489-494
ISSN:0009-918X
Container-title:Rinsho Shinkeigaku
language:en
Short-container-title:Rinsho Shinkeigaku

Author:

Sakiyama Yoshio¹,Watanabe Eri¹,Otsuka Mieko¹,Hirahara Taishi²,Momomura Shinichi²,Hayashi Yukiko³⁴

Affiliation:

1. Department of Neurology, Jichi Medical University, Saitama Medical Center

2. Department of Cardiovascular Medicine, Jichi Medical University, Saitama Medical Center

3. Department of Neuromuscular Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry (NCNP)

4. Department of Neurophysiology, Tokyo Medical University

Publisher

Societas Neurologica Japonica

Subject

Clinical Neurology

Link

https://www.jstage.jst.go.jp/article/clinicalneurol/54/6/54_489/_pdf

Reference13 articles.

1. 2) Hermans MC, Pinto YM, Merkies IS, et al. Hereditary muscular dystrophies and the heart. Neuromuscul Disord 2010;20:479-492.

2. 3) Bonne G, Di Barletta MR, Varnous S, et al. Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy. Nat Genet 1999;21:285-288.

3. 4) Raffaele Di Barletta M, Ricci E, Galluzzi G, et al. Different mutations in the LMNA gene cause autosomal dominant and autosomal recessive Emery-Dreifuss muscular dystrophy. Am J Hum Genet 2000;66:1407-1412.

4. 5) Sakata K, Shimizu M, Ino H, et al. High incidence of sudden cardiac death with conduction disturbances and atrial cardiomyopathy caused by a nonsense mutation in the STA gene. Circulation 2005;111:3352-3358.

5. 6) Muchir A, Bonne G, van der Kooi AJ, et al. Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B). Hum Mol Genet 2000;9:1453-1459.

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