Cargando…

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

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,...

Descripción completa

Detalles Bibliográficos
Autor principal: Fayssoil, Abdallah
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2576248/
https://www.ncbi.nlm.nih.gov/pubmed/18928563
http://dx.doi.org/10.1186/1749-8090-3-56
_version_ 1782160376793661440
author Fayssoil, Abdallah
author_facet Fayssoil, Abdallah
author_sort Fayssoil, Abdallah
collection PubMed
description 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.
format Text
id pubmed-2576248
institution National Center for Biotechnology Information
language English
publishDate 2008
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-25762482008-10-31 Should we perform systematic electrophysiological study in Steinert's disease? Fayssoil, Abdallah J Cardiothorac Surg Letters to the Editor 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. BioMed Central 2008-10-18 /pmc/articles/PMC2576248/ /pubmed/18928563 http://dx.doi.org/10.1186/1749-8090-3-56 Text en Copyright © 2008 Fayssoil; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Letters to the Editor
Fayssoil, Abdallah
Should we perform systematic electrophysiological study in Steinert's disease?
title Should we perform systematic electrophysiological study in Steinert's disease?
title_full Should we perform systematic electrophysiological study in Steinert's disease?
title_fullStr Should we perform systematic electrophysiological study in Steinert's disease?
title_full_unstemmed Should we perform systematic electrophysiological study in Steinert's disease?
title_short Should we perform systematic electrophysiological study in Steinert's disease?
title_sort should we perform systematic electrophysiological study in steinert's disease?
topic Letters to the Editor
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2576248/
https://www.ncbi.nlm.nih.gov/pubmed/18928563
http://dx.doi.org/10.1186/1749-8090-3-56
work_keys_str_mv AT fayssoilabdallah shouldweperformsystematicelectrophysiologicalstudyinsteinertsdisease