Evolution of cardiac abnormalities in Becker muscular dystrophy over a 13-year period

Hoogerwaard, E. M.; Voogt, Willem G. de; Wilde, Arthur A.M.; Wouw, Poll A. van der; Bakker, Egbert; Ommen, G.J.B. van; Visser, Marjolein

doi:10.1007/s004150050163

Cited by 56 publications

(42 citation statements)

References 39 publications

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“…There is no correlation between CI and the severity of skeletal muscle manifestations (14,16). There are also no correlations between the severity of CI and the deleted exons (4,17).…”

Section: Pathoanatomical Background Of CI In Bmdmentioning

confidence: 95%

“…Overall, CI is the rule rather than the exception in BMD (17). The onset of symptomatic CI is highly variable, but most frequently occurs in the third decade of life.…”

Section: Course and Outcome Of CI In Bmdmentioning

confidence: 99%

“…Left ventricular dilation may begin at any time during the course of the disease. In a study of 27 patients (17), the proportion of patients with ECG abnormalities increased from 44% to 71% over 12 years; 22% became symptomatic and four died of heart failure (17). The rate of progression is unpredictable.…”

Section: Course and Outcome Of CI In Bmdmentioning

confidence: 99%

“…In some cases, hCMP may rapidly progress to dCMP (6). A substantial proportion of patients develop incapacitating and life-threatening CMP (17). The most common causes of death in CI are arrhythmias or heart failure.…”

Section: Course and Outcome Of CI In Bmdmentioning

confidence: 99%

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Cardiac involvement in Becker muscular dystrophy

Finsterer¹,

Stöllberger²

2008

Canadian Journal of Cardiology

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“…There is no correlation between CI and the severity of skeletal muscle manifestations (14,16). There are also no correlations between the severity of CI and the deleted exons (4,17).…”

Section: Pathoanatomical Background Of CI In Bmdmentioning

confidence: 95%

“…Overall, CI is the rule rather than the exception in BMD (17). The onset of symptomatic CI is highly variable, but most frequently occurs in the third decade of life.…”

Section: Course and Outcome Of CI In Bmdmentioning

confidence: 99%

Section: Course and Outcome Of CI In Bmdmentioning

confidence: 99%

Section: Course and Outcome Of CI In Bmdmentioning

confidence: 99%

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Cardiac involvement in Becker muscular dystrophy

Finsterer¹,

Stöllberger²

2008

Canadian Journal of Cardiology

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“…28,30,31 Life expectancy is severely conditioned by the presence of the cardiomyopathy, closely related to the type of dystrophin gene mutation. 32,33 Heart transplantation is often required.…”

Section: Duchenne Cardiomyopathymentioning

confidence: 99%

Muscular Dystrophies: Key Elements for Everyday Diagnosis and Management

Palladino¹,

Nigro

Politano³

2013

Cardiogenetics

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Muscular dystrophies are a heterogeneous group of inherited disorders that share similar clinical features and dystrophic changes on muscle biopsy, associated with progressive weakness. Weakness may be noted at birth or develop in late adult life. In recent years, cardiac involvement has been observed in a growing number of genetic muscle diseases, and considerable progress has been made in understanding the relationships between disease skeletal muscle and cardiac muscle disease. This review will focus on the skeletal muscle diseases most commonly associated with cardiac complications that can be diagnosed by echocardiography, such as dystrophinopathies including Duchenne (DMD) and Becker (BMD) muscular dystrophies, cardiomyopathy of DMD/BMD carriers and X-L dilated cardiomyopathy.

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Cardiac Involvement in Bethlem Myopathy

Finsterer¹,

Stöllberger²

2007

Arch Neurol

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Evolution of cardiac abnormalities in Becker muscular dystrophy over a 13-year period

Cited by 56 publications

References 39 publications

Cardiac involvement in Becker muscular dystrophy

Cardiac involvement in Becker muscular dystrophy

Muscular Dystrophies: Key Elements for Everyday Diagnosis and Management

Cardiac Involvement in Bethlem Myopathy

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