Introduction: Duchenne Muscular Dystrophies (DMD) is a genetic muscle disorder that causes degeneration and atrophy of skeletal muscle and heart. Objective: The aim of this survey is accomplish an evaluation electrocardiographic and echocardiography in the patients bearers of Duchene Muscular Dystrophies (DMD), to observe which alterations, which the degree of cardiac compromising these patient present and the effectiveness of these exams in the evaluation cardiologic. Methods: Nine patients of the sex male bearers of DMD, with medium age of 14.12 ± 4.19 years, varying of 7 to 23 years were appraised. All were submitted to the evaluation physiotherapy and the cardiologic: electrocardiogram and echocardiogram. Results: The experimental condi...
Emery-Dreifuss muscular dystrophy (EDMD) is a rare X-linked muscular disease with a potentially leth...
Objectives: Cardiac involvement has been reported in carriers of dystrophin mutations giving rise to...
Heart lesion is characteristic in Duchenne’s muscular dystrophy, however there is no unanimous opini...
Introduction Duchenne Muscular Dystrophies (DMD) is a genetic muscle disorder that causes degenerati...
Background: Cardiac problems are common and are a major cause of death in both Duchenne muscular dys...
BackgroundDuchene muscular dystrophy is an x-linked recessive progressive muscular disease. It prese...
Fundamento: É conhecido o envolvimento cardíaco em pacientes com distrofia muscular de Duchenne (DMD...
Duchenne muscle dystrophy (DMD) accounts for over 80 percent of muscle dystrophies due to x-linked m...
A cross-sectional study in a cohort of DNA proven carriers of Duchenne (DMD) and Becker (BMD) muscul...
Background: Duchenne muscular dystrophy (DMD) is the most common childhood form of muscular dystroph...
BACKGROUND: Progressive cardiomyopathy (CMP) is one main cause of death in DMD. This cross-sectional...
<p><strong>Objective </strong> To explore the evolution of Duchenne muscular dystrophy (DMD) patient...
Cardiac complications are frequently diagnosed in Duchenne muscular dystrophy (DMD), clinical manife...
IntroductionCardiomyopathy is a common cause of morbidity and death in patients with Duchenne muscul...
Duchenne muscular dystrophy (DMD) is a genetic, progressive neuromuscular condition that is marked b...
Emery-Dreifuss muscular dystrophy (EDMD) is a rare X-linked muscular disease with a potentially leth...
Objectives: Cardiac involvement has been reported in carriers of dystrophin mutations giving rise to...
Heart lesion is characteristic in Duchenne’s muscular dystrophy, however there is no unanimous opini...
Introduction Duchenne Muscular Dystrophies (DMD) is a genetic muscle disorder that causes degenerati...
Background: Cardiac problems are common and are a major cause of death in both Duchenne muscular dys...
BackgroundDuchene muscular dystrophy is an x-linked recessive progressive muscular disease. It prese...
Fundamento: É conhecido o envolvimento cardíaco em pacientes com distrofia muscular de Duchenne (DMD...
Duchenne muscle dystrophy (DMD) accounts for over 80 percent of muscle dystrophies due to x-linked m...
A cross-sectional study in a cohort of DNA proven carriers of Duchenne (DMD) and Becker (BMD) muscul...
Background: Duchenne muscular dystrophy (DMD) is the most common childhood form of muscular dystroph...
BACKGROUND: Progressive cardiomyopathy (CMP) is one main cause of death in DMD. This cross-sectional...
<p><strong>Objective </strong> To explore the evolution of Duchenne muscular dystrophy (DMD) patient...
Cardiac complications are frequently diagnosed in Duchenne muscular dystrophy (DMD), clinical manife...
IntroductionCardiomyopathy is a common cause of morbidity and death in patients with Duchenne muscul...
Duchenne muscular dystrophy (DMD) is a genetic, progressive neuromuscular condition that is marked b...
Emery-Dreifuss muscular dystrophy (EDMD) is a rare X-linked muscular disease with a potentially leth...
Objectives: Cardiac involvement has been reported in carriers of dystrophin mutations giving rise to...
Heart lesion is characteristic in Duchenne’s muscular dystrophy, however there is no unanimous opini...