Patent Ductus Arteriosus
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Last Posted: Mar 14, 2023
- Epigenetic Evaluation of the TBX20 Gene and Environmental Risk Factors in Mexican Paediatric Patients with Congenital Septal Defects.
García-Flores Esbeidy, et al. Cells 2023 0 (4) - Cantú syndrome: Findings from 74 patients in the International Cantú Syndrome Registry.
Grange Dorothy K, et al. American journal of medical genetics. Part C, Seminars in medical genetics 2019 0 (4) 658-681 - Cardiac manifestations and gene mutations of patients with RASopathies in Taiwan.
Lee Chung-Lin, et al. American journal of medical genetics. Part A 2019 0 (2) 357-364 - [Genetic analysis of a child with 13q deletion syndrome featuring congenital heart disease].
Shen Nan, et al. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2019 0 (6) 620-623 - Interactions between PDA-associated polymorphisms and genetic ancestry alter ductus arteriosus gene expression.
Clyman Ronald I, et al. Pediatric research 2021 0 (4) 903-911 - The effects of ductal size on the severity of pulmonary hypertension in children with patent ductus arteriosus (PDA): a multi-center study.
Chinawa Josephat M, et al. BMC pulmonary medicine 2021 0 (1) 79 - Two genetic variants in NEXN and ABCC6 genes found in a patient with right coronary artery to right ventricle fistula combined with giant coronary aneurysm and patent ductus arteriosus.
Peng Yongxuan, et al. Frontiers in cardiovascular medicine 2022 0 1048795 - A novel KLF13 mutation underlying congenital patent ductus arteriosus and ventricular septal defect, as well as bicuspid aortic valve.
Abhinav Pradhan, et al. Experimental and therapeutic medicine 2022 0 (4) 311 - Genetic polymorphisms and risk for acute renal failure in preterm neonates.
Vásárhelyi Barna, et al. Pediatric nephrology (Berlin, Germany) 2005 0 (2) 132-5 - Randomized Trial on Echocardiography-Guided Ductus Arteriosus Treatment to Reduce Necrotizing Enterocolitis.
Bravo María Carmen, et al. Frontiers in pediatrics 2022 0 807712
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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 the CDC Office of Public Health Genomics 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, 2023
- Page last updated:Mar 31, 2023
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