Hintergrund: Die myotone Dystrophie Typ 1 (MD1) ist eine Multisystemerkrankung, die sich
häufig auch am Herzen manifestiert. Linksventrikuläre Hypertrabekulierung (LVHT) wurde …

Congenital left ventricular hypertrabeculation/noncompaction (LVHT) is a common feature of
neuromuscular disorders (NMDs). Most commonly LVHT is located in the apex and the …

Familial Left Ventricular Hypertrabeculation in Myotonic Dystrophy Type 1 Page 1 © Urban &
Vogel 2003 Herz 466 Herz 28 · 2003 · Nr. 5 © Urban & Vogel Familial Left Ventricular …

Introduction Left ventricular (LV) dysfunction is a major prognostic determinant in myotonic
dystrophy type 1 (DM 1). Therefore, markers of early‐stage LV impairment may be useful …

The number of CTG repeats in the myotonic dystrophy protein kinase gene on chromosome
19q13. 3 was 5 for the normal allele and 300 for the expanded allele. The daughter of the …

Background—Myotonic dystrophy type 2 (DM2) is a genetic disorder characterized by
skeletal muscle symptoms, metabolic changes, and cardiac involvement. Histopathologic …

BACKGROUND: Myotonic dystrophy type 1 (DM1) is a neurological disorder with known
cardiac involvement, including conduction disturbances, arrhythmias, and ventricular …

Background Myotonic dystrophy type 1 (MD1) is a neuromuscular disorder with potential
involvement of the heart and increased risk of sudden death. Considering the importance of …

Abstract Myotonic dystrophy type 2 (DM2) is a slowly progressive, autosomal-dominant
disease. This is a multisystemic disorder that affects the heart, which is one of the main …

Background Myotonic dystrophy type 1 (DM1) is associated with increased cardiac morbidity
and mortality. Therefore, assessment of cardiac involvement and risk stratification for sudden …