The Genetics of Human Congenital Coronary Vascular Anomalies.
| Autor: | Garrido AO; Hospital Materno Infantil-Hospital Carlos de Haya, Málaga, Spain., Picazo B; Hospital Materno Infantil-Hospital Carlos de Haya, Málaga, Spain., Guadix JA; Department of Animal Biology, Faculty of Sciences, University of Málaga, Málaga, Spain.; Instituto de Biomedicina de Málaga (IBIMA)-Plataforma BIONAND, Málaga, Spain., Ruiz-Villalba A; Department of Animal Biology, Faculty of Sciences, University of Málaga, Málaga, Spain.; Instituto de Biomedicina de Málaga (IBIMA)-Plataforma BIONAND, Málaga, Spain., Pérez-Pomares JM; Department of Animal Biology, Faculty of Sciences, University of Málaga, Málaga, Spain. jmperezp@uma.es.; Instituto de Biomedicina de Málaga (IBIMA)-Plataforma BIONAND, Málaga, Spain. jmperezp@uma.es. |
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| Jazyk: | angličtina |
| Zdroj: | Advances in experimental medicine and biology [Adv Exp Med Biol] 2024; Vol. 1441, pp. 811-816. |
| DOI: | 10.1007/978-3-031-44087-8_48 |
| Abstrakt: | The genetics of human congenital coronary vascular anomalies (hCCVA) remains largely underresearched. This is surprising, because although coronary vascular defects represent a relatively small proportion of human congenital heart disease (CHD), hCCVAs are clinically significant conditions. Indeed, hCCVA frequently associate to other congenital cardiac structural defects and may even result in sudden cardiac death in the adult. In this brief chapter, we will attempt to summarize our current knowledge on the topic, also proposing a rationale for the development of novel approaches to the genetics of hCCVA. (© 2024. The Author(s), under exclusive license to Springer Nature Switzerland AG.) |
| Databáze: | MEDLINE |
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