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CASE REPORT
Korean J Pediatr 2012 September;55(9) :350-353.
Published online 2012 September 14.        doi:https://doi.org/10.3345/kjp.2012.55.9.350
A case of Becker muscular dystrophy with early manifestation of cardiomyopathy
Ki Hyun Doo (Doo KH)1, Hye Won Ryu (Ryu HW)1, Seung Soo Kim (Kim SS)2, Byung Chan Lim (Lim BC)1, Hui Hwang (Hwang H)1, Ki Joong Kim (Kim KJ)1, Yong Seung Hwang (Hwang YS)1, Jong-Hee Chae (Chae JH)1
1Department of Pediatrics, Seoul National University College of Medicine, Seoul, Korea
2Department of Pediatrics, Soonchunhyang University College of Medicine, Cheonan, Korea
Corresponding Author: Jong-Hee Chae ,Tel: +82-2-2072-3622, Fax: +82-2-743-3455, Email: chaeped1@snu.ac.kr
Copyright © 2012 by The Korean Pediatric Society
ABSTRACT
An 18-year-old boy was admitted with chest discomfort, nausea, and dyspnea at rest. At the age of 3 years, he underwent muscle biopsy and dystrophin gene analysis owing to an enlarged calf muscle and elevated serum kinase level (6,378 U/L) without overt weakness; based on the results, Becker muscular dystrophy (BMD) was diagnosed. The dystrophin gene showed deletion of exons 45 to 49. He remained ambulant and could step upstairs without significant difficulties. A chest roentgenogram showed cardiomegaly (cardiothoracic ratio, 54%), and his electrocardiogram (ECG) showed abnormal ST-T wave, biatrial enlargement, and left ventricular hypertrophy. The 2-dimensional and M-mode ECGs showed a severely dilated left ventricular cavity with diffuse hypokinesis. The systolic indices were reduced, including fractional shortening (9%) and ejection fraction (19%). Despite receiving intensive medical treatment, he died from congestive heart failure 5 months after the initial cardiac symptoms. We report a case of BMD with early-onset dilated cardiomyopathy associated with deletion of exons 45 to 49. Early cardiomyopathy can occur in BMD patients with certain genotypes; therefore, careful follow-up is required even in patients with mild phenotypes of BMD.
Keywords: Becker muscular dystrophy | Early onset cardiomyopathy | Genotype
 
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