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Page 1
An Update on Pediatric Cardiomyopathy.
Choudhry S, Puri K, Denfield SW. Choudhry S, et al. Curr Treat Options Cardiovasc Med. 2019 Jun 25;21(8):36. doi: 10.1007/s11936-019-0739-y. Curr Treat Options Cardiovasc Med. 2019. PMID: 31236771 Review.
Dilated cardiomyopathy, characterized by left ventricular dilation and systolic dysfunction with normal left ventricular wall thickness, accounts for about 50-60% of all pediatric cardiomyopathy cases. This is followed by hypertrophic cardiomyop …
Dilated cardiomyopathy, characterized by left ventricular dilation and systolic dysfunction with normal left ventric …
Noncompaction cardiomyopathy: a current view.
Rosa LV, Salemi VM, Alexandre LM, Mady C. Rosa LV, et al. Arq Bras Cardiol. 2011 Jul;97(1):e13-9. doi: 10.1590/s0066-782x2011000900021. Arq Bras Cardiol. 2011. PMID: 21894393 Free article. Review. English, Portuguese, Spanish.
Isolated non-compaction cardiomyopathy is a rare disease that is likely to develop in the embryonic period. ...Even though this disease is said to be prevalent in the pediatric population or together with congenital heart disease, …
Isolated non-compaction cardiomyopathy is a rare disease that is likely to develop in the embryonic period. ...Even tho …
Echocardiographic Features of Cardiomyopathies: A Comprehensive Review.
Al-Naami GH. Al-Naami GH. Echocardiography. 2025 Oct;42(10):e70309. doi: 10.1111/echo.70309. Echocardiography. 2025. PMID: 41065104 Free PMC article. Review.
Cardiomyopathies represent a heterogeneous group of myocardial diseases characterized by structural and functional abnormalities that can lead to heart failure, arrhythmias, and sudden cardiac death. ...This review comprehensively outlines the echocard …
Cardiomyopathies represent a heterogeneous group of myocardial diseases characterized by structural and functional abnormalities that …
Myocardial and Arrhythmic Spectrum of Neuromuscular Disorders in Children.
Baban A, Lodato V, Parlapiano G, di Mambro C, Adorisio R, Bertini ES, Dionisi-Vici C, Drago F, Martinelli D. Baban A, et al. Biomolecules. 2021 Oct 25;11(11):1578. doi: 10.3390/biom11111578. Biomolecules. 2021. PMID: 34827576 Free PMC article. Review.
Their signs and symptoms are often multisystemic, with frequent cardiac involvement. In fact, childhood onset forms can predispose a person to various progressive cardiac abnormalities including cardiomyopathies (CMPs), valvulopathies, atrioventricular conduction de …
Their signs and symptoms are often multisystemic, with frequent cardiac involvement. In fact, childhood onset forms can predispose a …
A novel RYR2 loss-of-function mutation (I4855M) is associated with left ventricular non-compaction and atypical catecholaminergic polymorphic ventricular tachycardia.
Roston TM, Guo W, Krahn AD, Wang R, Van Petegem F, Sanatani S, Chen SR, Lehman A. Roston TM, et al. J Electrocardiol. 2017 Mar-Apr;50(2):227-233. doi: 10.1016/j.jelectrocard.2016.09.006. Epub 2016 Sep 8. J Electrocardiol. 2017. PMID: 27646203
BACKGROUND: Catecholaminergic polymorphic ventricular tachycardia (CPVT) is an ion channelopathy usually caused by gain-of-function mutations ryanodine receptor type-2 (RyR2). Left ventricular non-compaction (LVNC) is an often genetic cardiomyop …
BACKGROUND: Catecholaminergic polymorphic ventricular tachycardia (CPVT) is an ion channelopathy usually caused by gain-of-function m …
Left Ventricular Non-Compaction Cardiomyopathy: The Tragedies & Trabeculations of the Architectural Cardiac Sponge.
Ramazani N, Ivey B, Chakraborty S, Bishev D, DiCaro M, Duru P, Shao R, Singh A. Ramazani N, et al. J Clin Med. 2026 Mar 6;15(5):2023. doi: 10.3390/jcm15052023. J Clin Med. 2026. PMID: 41827439 Free PMC article. Review.
Left-ventricular non-compaction (LVNC) is a recently classified cardiomyopathy that involves abnormal trabeculations inside the left ventricle, most commonly located in the ventricular apex. There are 9 distinct types of non-com …
Left-ventricular non-compaction (LVNC) is a recently classified cardiomyopathy that involves abnormal trabeculat …
Copy Number Variants in Cardiac Channelopathies: Still a Missed Part in Routine Arrhythmic Diagnostics.
Gnazzo M, Parlapiano G, Di Lorenzo F, Perrino D, Genovese S, Lanari V, Righi D, Calì F, Silvetti MS, Falcone E, Bauleo A, Drago F, Novelli A, Baban A. Gnazzo M, et al. Biomolecules. 2024 Nov 15;14(11):1450. doi: 10.3390/biom14111450. Biomolecules. 2024. PMID: 39595626 Free PMC article.
CNVs in SCN5A were represented by the Brugada pattern, with major cardiac events mainly in males. Conversely, adult females show more supraventricular arrhythmias. RYR2-exon3 deletion showed a broader phenotype, including left ventricular non …
CNVs in SCN5A were represented by the Brugada pattern, with major cardiac events mainly in males. Conversely, adult females sh …
Sudden Cardiac Death in Children Affected by Cardiomyopathies: An Update on Risk Factors and Indications at Transvenous or Subcutaneous Implantable Defibrillators.
Rella V, Parati G, Crotti L. Rella V, et al. Front Pediatr. 2020 Apr 3;8:139. doi: 10.3389/fped.2020.00139. eCollection 2020. Front Pediatr. 2020. PMID: 32318526 Free PMC article. Review.
In the present paper, we will discuss the main cardiomyopathies affecting children with a specific focus on risk stratification and prevention of sudden cardiac death (SCD). We will discuss the main clinical features of hypertrophic cardiomyopathy (HCM), dilated and restri …
In the present paper, we will discuss the main cardiomyopathies affecting children with a specific focus on risk stratification and preventi …
Catheter ablation for patients with end-stage complex congenital heart disease or cardiomyopathy considered for transplantation: Trials and tribulations.
Cazzoli I, Gunturiz-Beltran C, Guarguagli S, Alonso-Gonzalez R, Babu-Narayan SV, Dimopoulos K, Swan L, Uebing A, Gatzoulis MA, Ernst S. Cazzoli I, et al. Int J Cardiol. 2020 Feb 15;301:127-134. doi: 10.1016/j.ijcard.2019.09.021. Epub 2019 Sep 10. Int J Cardiol. 2020. PMID: 31604655 Free article.
INTRODUCTION: Arrhythmia contributes significantly to morbidity and mortality of patients with congenital heart disease (CHD) or cardiomyopathy (CMP). ...METHODS: Five consecutive patients (3 female, mean age 47.8 12.8 years) with complex CHD or CMP (tricus …
INTRODUCTION: Arrhythmia contributes significantly to morbidity and mortality of patients with congenital heart disease …
Cardiovascular Involvement in Pediatric Laminopathies. Report of Six Patients and Literature Revision.
Baban A, Cicenia M, Magliozzi M, Gnazzo M, Cantarutti N, Silvetti MS, Adorisio R, Dallapiccola B, Bertini E, Novelli A, Drago F. Baban A, et al. Front Pediatr. 2020 Jul 24;8:374. doi: 10.3389/fped.2020.00374. eCollection 2020. Front Pediatr. 2020. PMID: 32793522 Free PMC article.
Cardiac involvement includes progressive arrhythmias (brady/tachyarrhythmias, sudden cardiac death). Furthermore, cardiomyocyte damage often progresses into dilated cardiomyopathy (DCM), rarely described in the pediatric age group. Neuromuscular manife …
Cardiac involvement includes progressive arrhythmias (brady/tachyarrhythmias, sudden cardiac death). Furthermore, cardi …
12 results