Should we perform systematic electrophysiological study in Steinert's disease?

نویسنده

  • Abdallah Fayssoil
چکیده

Myotonic dystrophy type 1 (Steinert's disease) is a multisystem disorder with autosomal dominant inheritance. This disease is associated with the presence of an abnormal expansion of a cytosine thymine-guanine (CTG) trinucleotide repeat on chromosome 19q13.3. Because of rhythmic complications, the place for systematic electrophysiological study (EPS) has to be discussed.

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عنوان ژورنال:
  • Journal of Cardiothoracic Surgery

دوره 3  شماره 

صفحات  -

تاریخ انتشار 2008