Mitral Valve Prolapse
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Last Posted: Jan 10, 2023
- Diagnosis and clinical presentation of two individuals with a rare TCF20 pathogenic variant.
Schneeweiss Michelle Robyn et al. BMJ case reports 2023 15(12) - A lightweight hybrid deep learning system for cardiac valvular disease classification.
Al-Issa Yazan et al. Scientific reports 2022 12(1) 14297 - Prevalence and potential genetic determinants of young sudden unexplained death victims with suspected arrhythmogenic mitral valve prolapse syndrome.
Giudicessi John R et al. Heart rhythm O2 2021 2(5) 431-438 - A multi-institutional experience in vascular Ehlers-Danlos syndrome diagnosis.
Shalhub Sherene et al. Journal of vascular surgery 2020 71(1) 149-157 - Marfan syndrome and related connective tissue disorders in the current era in Switzerland in 103 patients: medical and surgical management and impact of genetic testing.
Bombardieri Elisa et al. Swiss medical weekly 2020 Mar 150w20189 - Mitral valve prolapse, a familial condition worth screening for?
Regieli Jakub J et al. European journal of preventive cardiology 2019 Dec 2047487319893368 - CLINGEN Actionability Report for Arterial tortuosity syndrome - SLC2A10
ClinGen Actionability Working Group - CLINGEN Actionability Report for Autosomal Dominant Polycystic Kidney Disease - DNAJB11, GANAB, PKD1, PKD2
ClinGen Actionability Working Group - CLINGEN Actionability Report for Ehlers-Danlos Syndrome Type IV - COL3A1
ClinGen Actionability Working Group - CLINGEN Actionability Report for Ehlers-Danlos syndrome, classic type - COL5A1, COL5A2
ClinGen Actionability Working Group
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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.
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 25, 2024
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