Aims To assess the reported prevalence of left ventricular non-compaction (LVNC) in
different adult cohorts, taking in to consideration the role of diagnostic criteria and imaging …

Myotonic dystrophy type 1 (DM1), the most common muscular dystrophy affecting adults and
children, is a multi-systemic disorder affecting skeletal, cardiac, and smooth muscles as well …

Antecedentes y objetivos La enfermedad de Steinert o distrofia miotónica tipo 1
(DM1),(OMIM 160900) es la miopatía más prevalente en el adulto. Es una enfermedad …

Background and objectives Steinert's disease or myotonic dystrophy type 1 (MD1),(OMIM
160900), is the most prevalent myopathy in adults. It is a multisystemic disorder with …

Abstract Myotonic dystrophy type 1 (DM1), the most common adult muscular dystrophy, is an
autosomal dominant disorder caused by an expansion of a (CTG) n tract within the 3 …

CTG repeat expansion (CTG exp) is associated with aberrant alternate splicing that
contributes to cardiac dysfunction in myotonic dystrophy type 1 (DM1). Excision of this CTG …

Myotonic dystrophy type 1 (DM1) is the most common muscular dystrophy in adults. Cardiac
involvement is reported in 80% of cases and includes conduction disturbances, arrhythmias …

Myotonic dystrophy is a hereditary disorder with systemic involvement. The Italian Neuro-
Cardiology Network-“Rete delle Neurocardiologie”(INCN-RNC) is a unique collaborative …

Background Cardiac involvement in myotonic dystrophy type 1 (MD1) includes conduction
disease, arrhythmias, and left-ventricular (LV) systolic dysfunction leading to an increased …

Left ventricular noncompaction (LVNC) is a heterogeneous entity and, in reality, a likely
spectrum of disease which is clinically associated with arrhythmia, thromboembolic …