Excessive Trabeculation of the Left Ventricle: JACC: Cardiovascular Imaging Expert Panel Paper
Excessive trabeculation, often referred to as “noncompacted” myocardium, has been
described at all ages, from the fetus to the adult. Current evidence for myocardial …
described at all ages, from the fetus to the adult. Current evidence for myocardial …
The trouble with trabeculation: how genetics can help to unravel a complex and controversial phenotype
R Walsh - Journal of Cardiovascular Translational Research, 2023 - Springer
Excessive trabeculation of the cardiac left ventricular wall is a complex phenotypic substrate
associated with various physiological and pathological processes. There has been …
associated with various physiological and pathological processes. There has been …
Assessment of the diagnostic yield of combined cardiomyopathy and arrhythmia genetic testing
Importance Genetic testing can guide management of both cardiomyopathies and
arrhythmias, but cost, yield, and uncertain results can be barriers to its use. It is unknown …
arrhythmias, but cost, yield, and uncertain results can be barriers to its use. It is unknown …
Application of next-generation sequencing in cardiology: current and future precision medicine implications
E Papadopoulou, D Bouzarelou, G Tsaousis… - Frontiers in …, 2023 - frontiersin.org
Inherited cardiovascular diseases are highly heterogeneous conditions with multiple genetic
loci involved. The application of advanced molecular tools, such as Next Generation …
loci involved. The application of advanced molecular tools, such as Next Generation …
[HTML][HTML] Left ventricular noncompaction: a disorder with genotypic and phenotypic heterogeneity—a narrative review
K Hirono, F Ichida - Cardiovascular Diagnosis and Therapy, 2022 - ncbi.nlm.nih.gov
Left ventricular noncompaction: a disorder with genotypic and phenotypic heterogeneity—a
narrative review - PMC Back to Top Skip to main content NIH NLM Logo Access keys NCBI …
narrative review - PMC Back to Top Skip to main content NIH NLM Logo Access keys NCBI …
[HTML][HTML] Genetic landscape in Russian patients with familial left ventricular noncompaction
AN Meshkov, RP Myasnikov, AV Kiseleva… - Frontiers in …, 2023 - frontiersin.org
Left ventricular noncompaction (LVNC) cardiomyopathy is a disorder that can be
complicated by heart failure, arrhythmias, thromboembolism, and sudden cardiac death. The …
complicated by heart failure, arrhythmias, thromboembolism, and sudden cardiac death. The …
Multidisciplinary approach in cardiomyopathies: From genetics to advanced imaging
F Santoro, E Vitale, I Ragnatela, R Cetera… - Heart Failure …, 2024 - Springer
Cardiomyopathies are myocardial diseases characterized by mechanical and electrical
dysfunction of the heart muscle which could lead to heart failure and life-threatening …
dysfunction of the heart muscle which could lead to heart failure and life-threatening …
Role of TBX20 Truncating Variants in Dilated Cardiomyopathy and Left Ventricular Noncompaction
A Amor-Salamanca, A Santana Rodríguez… - Circulation: Genomic …, 2024 - Am Heart Assoc
BACKGROUND: Less than 40% of patients with dilated cardiomyopathy (DCM) have a
pathogenic/likely pathogenic genetic variant identified. TBX20 has been linked to congenital …
pathogenic/likely pathogenic genetic variant identified. TBX20 has been linked to congenital …
[HTML][HTML] Advances and Challenges in the Diagnosis and Management of Left Ventricular Noncompaction in Adults: A Literature Review
J Llerena-Velastegui, S Velastegui-Zurita… - Current Problems in …, 2024 - Elsevier
In the realm of cardiovascular health, isolated left ventricular noncompaction (LVNC) stands
out for its distinct morphological features and the clinical challenges it presents, particularly …
out for its distinct morphological features and the clinical challenges it presents, particularly …
Unusual Evolution of Hypertrophic Cardiomyopathy in Non-Compaction Myocardium in a Pompe Disease Patient
V Gragnaniello, C Rizzardi, A Commone… - Journal of Clinical …, 2023 - mdpi.com
Classic infantile Pompe disease is characterized by a severe phenotype with
cardiomyopathy and hypotonia. Cardiomyopathy is generally hypertrophic and rapidly …
cardiomyopathy and hypotonia. Cardiomyopathy is generally hypertrophic and rapidly …