… mitochondrial disorders, Barth syndrome, zaspopathy, and myotonic dystrophy type 1. LVHT
does not seem to be a special type of cardiac involvement of NMDs. NMDs affect prognosis …

… 2 9 Survival curves (death or cardiac transplantation) of 126 patients with the dilated phenotype
of left ventricular hypertrabeculation/ noncompaction depending on presence (light blue) …

… J.,et al.,2014), and left ventricular hypertrabeculation (LVHT), … abnormalities in patients with
myotonic dystrophy type 1. Clin Res … , myotonic myopathy and hypotension traits of myotonic …

… Though rarely occurring in MD2 [3], we should be informed how many of the included patients
presented with left ventricular hypertrabeculation (LVHT), also known as noncompaction …

… this fetus developed 1 week later. Forty-eight hours after delivery, left ventricular EF reduced
… same patient demonstrated progressive left ventricular dilatation with an left ventricular end-…

… Although left ventricular dysfunction was frequently detected in patients with VT, the only …
Additional structural abnormalities such as hypertrabeculation fulfilling noncompaction criteria …

… develop systolic or diastolic dysfunction or left ventricular hypertrabeculation, also known as
… in myotonic dystrophy type 1 (Steinert disease) ... when there is an indication of ventricular …

… like Myotonic dystrophies and Cobalamin … ventricular hypertrabeculation in the development
of LVNC. While gain of function mutations in certain genes and resulting hypertrabeculation …

… Most frequently associated with LVHT are mitochondrial disorders, Barth syndrome, zaspopathy,
myotonic dystrophy type 1, dystrobrevinopathy and Emery-Dreifuss muscular dystrophy …

… hyper trabeculation/noncompaction, which is indistinguishable from congenital noncompaction,
has been reported in highly trained athletes [50], patients with myotonic dystrophy [51], …