Should we perform systematic electrophysiological study in Steinert's disease?
| Author(s) : | Abdallah Fayssoil, |
| Publisher : | N/A |
| Publication Date : | 2008 |
| ISSN : | N/A |
| Abstract : | Abstract 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. , |