Excessive Trabeculation of the Left Ventricle: JACC: Cardiovascular Imaging Expert Panel Paper

SE Petersen, B Jensen, N Aung, MG Friedrich… - Cardiovascular …, 2023 - jacc.org
Excessive trabeculation, often referred to as “noncompacted” myocardium, has been
described at all ages, from the fetus to the adult. Current evidence for myocardial …

Left ventricular noncompaction: a distinct genetic cardiomyopathy?

E Arbustini, V Favalli, N Narula, A Serio… - Journal of the American …, 2016 - jacc.org
Left ventricular noncompaction (LVNC) describes a ventricular wall anatomy characterized
by prominent left ventricular (LV) trabeculae, a thin compacted layer, and deep …

Novel genetic triggers and genotype–phenotype correlations in patients with left ventricular noncompaction

K Miszalski-Jamka, JL Jefferies, W Mazur… - Circulation …, 2017 - Am Heart Assoc
Background—Left ventricular noncompaction (LVNC) is a genetically and phenotypically
heterogeneous disease and, although increasingly recognized in clinical practice, there is a …

[HTML][HTML] Left ventricular noncompaction cardiomyopathy

DP Singh, H Patel - StatPearls [Internet], 2022 - ncbi.nlm.nih.gov
Objectives: Review the etiology of left ventricular non-compaction cardiomyopathy. Describe
the evaluation of left ventricular non-compaction cardiomyopathy. Summarize the treatment …

[HTML][HTML] Barth syndrome

C Ferreira, G Pierre, R Thompson, H Vernon - 2020 - europepmc.org
Barth syndrome is characterized in affected males by cardiomyopathy, neutropenia, skeletal
myopathy, prepubertal growth delay, and distinctive facial gestalt (most evident in infancy); …

Cardiac MRI biomarkers for Duchenne muscular dystrophy

P Magrath, N Maforo, P Renella, SF Nelson… - Biomarkers in …, 2018 - Taylor & Francis
Duchenne muscular dystrophy (DMD) is a fatal inherited genetic disorder that results in
progressive muscle weakness and ultimately loss of ambulation, respiratory failure and …

Effect of the Non-Immunosuppressive MPT Pore Inhibitor Alisporivir on the Functioning of Heart Mitochondria in Dystrophin-Deficient mdx Mice

MV Dubinin, VS Starinets, EY Talanov, IB Mikheeva… - Biomedicines, 2021 - mdpi.com
Supporting mitochondrial function is one of the therapeutic strategies that improve the
functioning of skeletal muscle in Duchenne muscular dystrophy (DMD). In this work, we …

Interventions for preventing and treating cardiac complications in Duchenne and Becker muscular dystrophy and X‐linked dilated cardiomyopathy

JP Bourke, T Bueser… - Cochrane Database of …, 2018 - cochranelibrary.com
Background The dystrophinopathies include Duchenne muscular dystrophy (DMD), Becker
muscular dystrophy (BMD), and X‐linked dilated cardiomyopathy (XLDCM). In recent years …

Left Ventricular Non-Compaction in Children: Aetiology and Diagnostic Criteria

E Monda, G De Michele, G Diana, F Verrillo, M Rubino… - Diagnostics, 2024 - mdpi.com
Left ventricular non-compaction (LVNC) is a heterogeneous myocardial disorder
characterized by prominent trabeculae protruding into the left ventricular lumen and deep …

Trabeculations of the porcine and human cardiac ventricles are different in number but similar in total volume

B Jensen, D Salvatori, J Schouten… - Clinical …, 2024 - Wiley Online Library
An intricate meshwork of trabeculations lines the luminal side of cardiac ventricles.
Compaction, a developmental process, is thought to reduce trabeculations by adding them …