Long Qt Syndrome 1
What's New
Last Posted: Mar 21, 2024
- Diagnostic yield from cardiac gene testing for inherited cardiac conditions and re-evaluation of pre-ACMG variants of uncertain significance.
Jane Murphy et al. Ir J Med Sci 2024 - Deep Learning-Augmented ECG Analysis for Screening and Genotype Prediction of Congenital Long QT Syndrome.
River Jiang et al. JAMA Cardiol 2024 - "Inherited cardiovascular disease mindset" can identify concealed inherited conditions at cardio-oncology evaluation: An opportunistic screening.
Rebeca Lorca et al. Int J Cardiol 2024 131825 - Unraveling Complexities in Genetically Elusive Long QT Syndrome.
Babken Asatryan et al. Circ Arrhythm Electrophysiol 2024 e012356 - Assessment of Sudden Cardiac Death Risk in Pediatric Primary Electrical Disorders: A Comprehensive Overview.
Adelina Pupaza et al. Diagnostics (Basel) 2023 13(23) - Real-world utilization of guideline-directed genetic testing in inherited cardiovascular diseases.
Mauro Longoni et al. Front Cardiovasc Med 2023 101272433 - Return-to-Play for Elite Athletes With Genetic Heart Diseases Predisposing to Sudden Cardiac Death.
Katherine A Martinez et al. J Am Coll Cardiol 2023 82(8) 661-670 - hERG agonists pose challenges to web-based machine learning methods for prediction of drug-hERG channel interaction.
Aziza E L Harchi et al. J Pharmacol Toxicol Methods 2023 107293 - EMQN: Recommendations for genetic testing in inherited cardiomyopathies and arrhythmias.
Jesse B Hayesmoore et al. Eur J Hum Genet 2023 - The diagnostic value of electrocardiogram-based machine learning in long QT syndrome: a systematic review and meta-analysis.
Min-Juan Wu et al. Front Cardiovasc Med 2023 101172451
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Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
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.
- Page last reviewed:Feb 1, 2024
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