… were metabolic myopathies, Barth syndrome, zaspopathy, myotonic dystrophy type 1,
dystrobrevinopathy, and Emery–Dreifuss muscular dystrophy [Citation81]. Unfortunately, there is …

… myotonic dystrophies (Table 1) (Meola, 2000). The myotonic dystrophies comprise myotonic
dystrophy type 1 (DM1, classical form), myotonic dystrophy type 2 (DM2), and at least one …

… Myocardial fibrosis in patients with myotonic dystrophy type 1… 1] We agree with the points
highlighted regarding the etiology and clinical presentation of left ventricular hypertrabeculation …

… Transthoracic echocardiography, carried out for left bundle-branch-block and hyper-CK-…
surprisingly LVHT affecting the left ventricular apex and apical lateral wall (Fig. 1). The number …

… Myoadenylate-deaminase gene mutation associated with left ventricular hypertrabeculation. …
Left ventricular hypertrabeculation in myotonic dystrophy type 1. Herz 2001; 26: 287-90. 16. …

… So far, LVHT has been reported in association with NMDs like dystrophinopathy, myotonic
dystrophy 1, dystrobrevinopathy, Pompe's disease, myo-adenylate deaminase deficiency, …

… It is noteworthy that a mutation in the α-DB gene was reported in a family with left ventricular
noncompaction, 32 a cardiac abnormality associated with arrhythmia that occurs in some …

… dystrophy, Barth syndrome, mitochondriopathy, dystrobrevinopathy, myotonic dystrophy
type 1 and type … -deaminase deficiency, Duchenne muscular dystrophy, CharcotMarie-Tooth …

… , myotonic dystrophies type 1 and 2, proximal myotonic myopathy, myoadenylate deaminase
deficiency, glycogenosis type … thickening, left ventricular hypertrabeculation, dilatation of the …

… Noncompaction cardiomyopathy (NCCM), also known as left ventricular hypertrabeculation
(… between >75 and up to 11,000 repeats causes myotonic dystrophy type-2 (MD2) . MD2 is a …