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 …

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

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 …

Involvement of the cardiac conduction system is a common clinical feature in myotonic
dystrophy, whereas the association of primary myocardial abnormalities has rarely been …

Cardiac involveent in type 1 myotonic dystrophy. - Abstract - Europe PMC Sign in | Create an
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Structural alterations of the myocardium, such as fibrosis and fatty infiltration, were observed
in post-mortem examinations in patients with myotonic dystrophy, a familial multisystem …

To the Editor In a recent issue of JAMA Cardiology, we read with great interest the report of
Tanawuttiwat et al1 entitled “Left Ventricular Dysfunction and Conduction Disturbances in …

Abstract Myotonic dystrophy type 1 (DM1) is the commonest muscular dystrophy in adults,
affecting multiple organs in addition to skeletal muscles. Cardiac conduction system …

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

Background—Mutations in the genes encoding sarcomere proteins have been associated
with both hypertrophic and dilated cardiomyopathy. Recently, mutations in myosin heavy …