Heart Block
What's New
Last Posted: Mar 06, 2023
- Congenital second-degree heart block and total anomalous pulmonary venous return associated with microduplication of 1q32.2.
Puvabanditsin Surasak, et al. Annals of pediatric cardiology 2018 0 (2) 194-196 - A newly identified missense mutation in CLCA2 is associated with autosomal dominant cardiac conduction block.
Mao Zhuo, et al. Gene 2019 0 143990 - Complete Heart Block Secondary to Flecainide Toxicity: Is It Time for CYP2D6 Genotype Testing?
Poh Bao Hui, et al. Pediatrics 2020 0 (1) - High Prevalence of Late-Onset Fabry Cardiomyopathy in a Cohort of 499 Non-Selective Patients with Left Ventricular Hypertrophy: The Asian Fabry Cardiomyopathy High-Risk Screening Study (ASIAN-FAME).
Fan Yiting, et al. Journal of clinical medicine 2021 5 (10) - Role of family history and clinical screening in the identification of families with idiopathic dilated cardiomyopathy in Johannesburg, South Africa.
Bailly C et al. South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde 2019 Aug 109(9) 673-678 - Association of Natural Killer Cell Ligand Polymorphism HLA-C Asn80Lys With the Development of Anti-SSA/Ro-Associated Congenital Heart Block.
Ainsworth Hannah C, et al. Arthritis & rheumatology (Hoboken, N.J.) 2017 0 (11) 2170-2174 - PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity.
van Setten Jessica, et al. Nature communications 2018 0 (1) 2904 - Investigating Potential Correlations between Endodontic Pathology and Cardiovascular Diseases Using Epidemiological and Genetic Approaches.
Messing Maria, et al. Journal of endodontics 2019 1 - [Automatic Identifcation of Heart Block Precise Location Based on Sparse Connection Residual Network].
Qi Ji et al. Zhongguo yi liao qi xie za zhi = Chinese journal of medical instrumentation 2019 Mar 43(2) 86-89 - Genotypic and phenotypic predictors of complete heart block and recovery of conduction after surgical repair of congenital heart disease.
Murray Laura, et al. Heart rhythm : the official journal of the Heart Rhythm Society 2016 11 - Common Variants in the TBX5 Gene Associated with Atrial Fibrillation in a Chinese Han Population.
Zhang Rongfeng, et al. PloS one 2016 0 (8) e0160467 - Association Between Genetic Variation in the SCN10A Gene and Cardiac Conduction Abnormalities in Patients With Hypertrophic Cardiomyopathy.
Iio Chiharuko, et al. International heart journal 2015 0 (4) 421-7 - The HLA locus contains novel foetal susceptibility alleles for congenital heart block with significant paternal influence.
Meisgen S, et al. Journal of internal medicine 2014 6 (6) 640-51 - Heart Block
From NHLBI health topic site - The electrocardiographic features associated with cardiac amyloidosis of variant transthyretin isoleucine 122 type in Afro-Caribbean patients.
Dungu J, et al. American heart journal 2012 7 (1) 1 - Incidence of cardiac arrhythmias in asymptomatic hereditary hemochromatosis subjects with C282Y homozygosity.
Shizukuda Y, et al. The American journal of cardiology 2011 12 - Congenital heart block
From NCATS Genetic and Rare Diseases Information Center - Progressive familial heart block type 1A
From NCATS Genetic and Rare Diseases Information Center - Progressive familial heart block type 1B
From NCATS Genetic and Rare Diseases Information Center - Progressive familial heart block type 2
From NCATS Genetic and Rare Diseases Information Center - Genetic variation in SCN10A influences cardiac conduction.
Chambers John C, et al. Nature genetics 2010 2 (2) 149-52 - ACE I/D polymorphism associated with abnormal atrial and atrioventricular conduction in lone atrial fibrillation and structural heart disease: implications for electrical remodeling.
Watanabe Hiroshi, et al. Heart rhythm : the official journal of the Heart Rhythm Society 2009 9 (9) 1327-32 - Analysis of Single Nucleotide Polymorphisms (SNPs) of the small-conductance calcium activated potassium channel (SK3) gene as genetic modifier of the cardiac phenotype in myotonic dystrophy type 1 patients.
Rinaldi F, et al. Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology / edited by the Gaetano Conte Academy for the study of striated muscle diseases 2008 12 82-9 - Genetic association of cutaneous neonatal lupus with HLA class II and tumor necrosis factor alpha: implications for pathogenesis.
Clancy Robert M, et al. Arthritis and rheumatism 2004 8 (8) 2598-603 - Cytokine polymorphisms and histologic expression in autopsy studies: contribution of TNF-alpha and TGF-beta 1 to the pathogenesis of autoimmune-associated congenital heart block.
Clancy Robert M, et al. Journal of immunology (Baltimore, Md. : 1950) 2003 9 (6) 3253-61
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HLBS-PopOmics is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other materials that address the translation of genomic and other precision health discoveries into improved health care and prevention related to Heart and Vascular Diseases(H), Lung Diseases(L), Blood Diseases(B), and Sleep Disorders(S)...more
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Mensah GA, Yu W, Barfield WL, Clyne M, Engelgau MM, Khoury MJ. HLBS-PopOmics: an online knowledge base to accelerate dissemination and implementation of research advances in population genomics to reduce the burden of heart, lung, blood, and sleep disorders. Genet Med. 2018 Sep 10. doi: 10.1038/s41436-018-0118-1
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
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- Page last updated:May 18, 2024
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