The authors present two cases of myotonic dystrophy (Steinert's disease) with cardiac involvement in young adults. They point out the rareness of this disease, the multisystemic involvement and also the diagnostic problems in the absence of the classic clinical picture.The authors present two cases of myotonic dystrophy (Steinert's disease) with cardiac involvement in young adults. They point out the rareness of this disease, the multisystemic involvement and also the diagnostic problems in the absence of the classic clinical picture
BACKGROUND: Myotonic dystrophy (DM) is an inherited progressive muscle disorder caused by defects in...
Myotonic dystrophy type 1 (DM1, Steinert's syndrome) is an autosomal dominant disorder characterized...
Ambulatory electrocardiographic monitoring (AEM) was performed in 22 patients (range 13-62 years; me...
Myotonic dystrophy is frequently associated with cardiac abnormalities including defects of the card...
Myotonic dystrophy (MD) is associated with a wide spectrum of cardiac abnormalities, but only a few ...
Myotonic dystrophy (Dystrophia Myotonica, DM) is the most frequently inherited neuromuscular diseas...
Myotonic dystrophy type I or Steinert's disease is of autosomal dominant genetic origin. It is chara...
Steinerts disease or myotonic dystrophy type 1 is a genetic neuromuscular disorder with autosomal do...
17 patients with myotonic dystrophy have been studied. The skeletal muscle disease has been assessed...
Steinert's disease or myotonic dystrophy type 1 (MD1), (OMIM 160900), is the most prevalent myopathy...
Myotonic dystrophy (dystrophia myotonica, DM) is the most frequently inheritedneuromuscular disease ...
Myotonic dystrophy is an inherited systemic disorder affecting skeletal muscle and the heart. Geneti...
Myotonic dystrophy type 1 (DM1) is the commonest muscular dystrophy in adults, affecting multiple or...
Myotonic dystrophy type 1 (MD) is the most common autosomal dominant muscular dystro-phy in adults. ...
Type 1 myotonic dystrophy or DM1 (Steinert's disease), which is the commonest muscular dystrophy in ...
BACKGROUND: Myotonic dystrophy (DM) is an inherited progressive muscle disorder caused by defects in...
Myotonic dystrophy type 1 (DM1, Steinert's syndrome) is an autosomal dominant disorder characterized...
Ambulatory electrocardiographic monitoring (AEM) was performed in 22 patients (range 13-62 years; me...
Myotonic dystrophy is frequently associated with cardiac abnormalities including defects of the card...
Myotonic dystrophy (MD) is associated with a wide spectrum of cardiac abnormalities, but only a few ...
Myotonic dystrophy (Dystrophia Myotonica, DM) is the most frequently inherited neuromuscular diseas...
Myotonic dystrophy type I or Steinert's disease is of autosomal dominant genetic origin. It is chara...
Steinerts disease or myotonic dystrophy type 1 is a genetic neuromuscular disorder with autosomal do...
17 patients with myotonic dystrophy have been studied. The skeletal muscle disease has been assessed...
Steinert's disease or myotonic dystrophy type 1 (MD1), (OMIM 160900), is the most prevalent myopathy...
Myotonic dystrophy (dystrophia myotonica, DM) is the most frequently inheritedneuromuscular disease ...
Myotonic dystrophy is an inherited systemic disorder affecting skeletal muscle and the heart. Geneti...
Myotonic dystrophy type 1 (DM1) is the commonest muscular dystrophy in adults, affecting multiple or...
Myotonic dystrophy type 1 (MD) is the most common autosomal dominant muscular dystro-phy in adults. ...
Type 1 myotonic dystrophy or DM1 (Steinert's disease), which is the commonest muscular dystrophy in ...
BACKGROUND: Myotonic dystrophy (DM) is an inherited progressive muscle disorder caused by defects in...
Myotonic dystrophy type 1 (DM1, Steinert's syndrome) is an autosomal dominant disorder characterized...
Ambulatory electrocardiographic monitoring (AEM) was performed in 22 patients (range 13-62 years; me...