Hostname: page-component-cd9895bd7-jkksz Total loading time: 0 Render date: 2024-12-26T17:01:51.649Z Has data issue: false hasContentIssue false
  • English
  • Français

A rare prenatal diagnosis: congenital absence of aortic valve

Part of: Echocardiography

Published online by Cambridge University Press:  24 March 2022

Pelin Ayyildiz ,
Merve M. Aydemir Open the ORCID record for Merve M. Aydemir [Opens in a new window]  and
Alper Guzeltas Open the ORCID record for Alper Guzeltas [Opens in a new window]
Pelin Ayyildiz
Affiliation:
Department of Pediatric Cardiology, University of Health Sciences, Istanbul Mehmet Akif Ersoy Thoracic and Cardiovascular Surgery Training and Research Hospital, Istanbul, Turkey
Merve M. Aydemir*
Affiliation:
Department of Pediatric Cardiology, University of Health Sciences, Istanbul Mehmet Akif Ersoy Thoracic and Cardiovascular Surgery Training and Research Hospital, Istanbul, Turkey
Alper Guzeltas
Affiliation:
Department of Pediatric Cardiology, University of Health Sciences, Istanbul Mehmet Akif Ersoy Thoracic and Cardiovascular Surgery Training and Research Hospital, Istanbul, Turkey
*
Author for correspondence: M. M. Aydemir, Department of Pediatric Cardiology, University of Health Sciences, Istanbul Mehmet Akif Ersoy Thoracic and Cardiovascular Surgery Training and Research Hospital, Bezirganbahce Street, Halkali, Istanbul 34303, Turkey. Tel: +90 212 692 20 00. Fax: +90 212 471 80 03. E-mail: maze_zabun@hotmail.com
Get access Rights & Permissions [Opens in a new window]

Abstract

Congenital absence of the aortic valve is characterised by the absence of aortic valve and severe regurgitation. The rest of the reported cases were mostly diagnosed either on postnatal echocardiography or autopsy. Here, we present a foetal case with the absence of the aortic valve and “inverse circulatory shunt”.

Keywords

Aortic valve absencecongenital heart defectfoetal echocardiographyprenatal diagnosisinverse circulatory shunt
Type
Brief Report
Information
Cardiology in the Young , Volume 32 , Issue 12 , December 2022 , pp. 2018 - 2020
Check for updates
Copyright
© The Author(s), 2022. Published by Cambridge University Press

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Qasim, A, Johnson, CB, Aly, MA, et al. Prenatal diagnosis and successful palliation of absent aortic valve with hypoplastic left heart syndrome: a case report and review of literature. AJP Rep 2019; 9: e121–e126.Google ScholarPubMed
Yu, R, Li, SL, Luo, GY, et al. First-trimester echocardiographic features and perinatal outcomes in fetuses with congenital absence of the aortic valve. J Ultrasound Med 2016; 35: 739–745.CrossRefGoogle ScholarPubMed
Harada, Y, Takeuchi, T, Satomi, G, et al. Absent aortic valve: successful palliation in the neonate. Ann Thorac Surg 1998; 66: 935–936.CrossRefGoogle ScholarPubMed
Krasemann, T, Kehl, HG, Hammel, D, et al. Congenital aortic regurgitation due to absent aortic cusps and high-degree mitral stenosis. Pediatr Cardiol 2003; 24: 304–306.Google ScholarPubMed
Bierman, FZ, Yeh, MN, Swersky, S, et al. Absence of the aortic valve: antenatal and postnatal two-dimensional and Doppler echocardiographic features. J Am Coll Cardiol 1984; 3: 833–837.CrossRefGoogle ScholarPubMed
Murakami, T, Lin, L, Ishiodori, T, et al. Prenatal diagnosis of congenital absence of aortic valve associated with restrictive foramen ovale: hemodynamic features and clinical outcome. J Clin Ultrasound 2019; 47: 104–106.CrossRefGoogle ScholarPubMed
Murakami, T, Horigome, H, Shiono, J, et al. Prenatal diagnosis of congenital absence of aortic valve: a report of two cases with different outcomes and a literature review. Fetal Diagn Ther 2015; 38: 307–314.CrossRefGoogle ScholarPubMed
Goltz, D, Lunkenheimer, JM, Abedini, M, et al. Left ventricular obstruction with restrictive inter-atrial communication leads to retardation in fetal lung maturation. Prenat Diagn 2015; 35: 463–470.CrossRefGoogle ScholarPubMed

Ayyildiz et al. supplementary material

Ayyildiz et al. supplementary material 1

Download Ayyildiz et al. supplementary material(Video)
Video 2.4 MB

Ayyildiz et al. supplementary material

Ayyildiz et al. supplementary material 2

Download Ayyildiz et al. supplementary material(Video)
Video 1 MB