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Case report of rare congenital cardiovascular anomalies associated with truncus arteriosus type 2

  • Truncus arteriosus (TA) is a very rare congenital anomaly with complex cardiovascular anatomy and high lethality also due to severe associated anatomical variants and pathologies. As TA has a massive impact on the survival of a newborn and usually has to be surgically treated. Thus, it is of high importance to understand this congenital cardiovascular disease and associated complications, to improve life expectancy and outcome of these patients. We recently came across a newborn female patient with a rare complex case of persistent TA type 2 associated with further complex cardiovascular anomalies, who received a contrast enhanced CT scan on the 3 rd day post-partum, showing complex cardiovascular abnormalities that were ultimately incompatible with life.

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Author:Leona Soraja AlizadehORCiDGND, Vitali KochORCiDGND, Leon David GrünewaldORCiDGND, Ibrahim YelORCiDGND, Daniel Mathies, Dominic RauschningORCiDGND, Thomas J. VoglORCiDGND, Christian BoozORCiDGND
URN:urn:nbn:de:hebis:30:3-783609
DOI:https://doi.org/10.1016/j.heliyon.2022.e11033
ISSN:2405-8440
Parent Title (English):Heliyon
Publisher:Elsevier
Place of publication:Amsterdam
Document Type:Article
Language:English
Date of Publication (online):2022/10/14
Date of first Publication:2022/10/12
Publishing Institution:Universitätsbibliothek Johann Christian Senckenberg
Release Date:2023/10/17
Tag:Cardiovascular diseases; Congenital; Fetal heart; Heart defects; Truncus arteriosus
Volume:8
Issue:10, e11033
Article Number:e11033
Page Number:4
HeBIS-PPN:516008943
Institutes:Medizin
Dewey Decimal Classification:6 Technik, Medizin, angewandte Wissenschaften / 61 Medizin und Gesundheit / 610 Medizin und Gesundheit
Sammlungen:Universitätspublikationen
Licence (German):License LogoCreative Commons - CC BY-NC-ND - Namensnennung - Nicht kommerziell - Keine Bearbeitungen 4.0 International