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HERDIN Record #: PCHRD14111205301646 Submitted: 12 November 2014 Modified: 05 October 2018

Dilated cardiomyopathy in becker muscular dystrophy: A case report

Philipp C. Ines,
Philipp C. Ines,
Jose Donato A. Magno,
Jose Donato A. Magno,
Ronaldo C. Manuel,
Ronaldo C. Manuel,
Abdias V. Aquino,
Abdias V. Aquino

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BACKGROUND: Becker muscular dystrophy (BMD) is a rare X-linked muscular dystrophy, with an incidence of 3 in 100,000 live male births. The most common cardiac presentation is cardiomyopathy (occurs 50% of cases) and conduction disorders.

CASE: This is a case of a 27 year-old male who was diagnosed with BMD during his childhood. He developed gradual progressive muscle weakness with decrease in basal functional capacity. Dilated cardiomyopathy was observed based on clinical and echocardiographic findings. He was later admitted due to ventricular tachycardia. Upon admission, the chest x-ray showed cardiomegaly. Laboratory examination showed markedly elevated creatine phosphokinase (CPK) isoenzymes. Two-dimensional echocardiography showed generalized hypokinesia with severely depressed systolic function; and dilated left ventricular cavity and left atrium. The hospital course of the patient is herein described.

Publication Type
Publication Sub Type
Case report
Philippine Journal of Cardiology
Publication Date
January-June 2013
LocationLocation CodeAvailable FormatAvailability
Philippine Council for Health Research and Development Library Box No. 43 Fulltext Print Format
Philippine Heart Association Fulltext pdf (Download)

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