Williams Syndrome and Neonatal Cardiac Surgery for Congenital Single Ventricle

Authors

Taylor E. Katt, University of Nebraska Medical Center
Robert L. Spicer, Children's Hospital and Medical Center
Anji T. Yetman, University of Nebraska Medical CenterFollow
Ali N. Ibrahimiye, University of Nebraska Medical CenterFollow
James M. Hammel, Children's Hospital and Medical Center
Jeffrey A. Robinson, University of Nebraska Medical CenterFollow

Document Type

Article

Journal Title

JACC: Case Reports

Publication Date

2020

Volume

2

Abstract

Williams syndrome (WS) is an arteriopathic derangement associated with supravalvular aortic stenosis and branch pulmonary stenosis. We describe double-outlet right ventricle with mitral atresia and aortic arch hypoplasia in an infant with WS. This case demonstrates the difficulty in managing patients with WS with complex cardiac defects. To our knowledge, this is the first reported single-ventricle physiology in a patient with WS. (Level of Difficulty: Advanced.).

DOI Link

10.1016/j.jaccas.2020.05.098

ISSN

2666-0849

Creative Commons License

This work is licensed under a Creative Commons Attribution-NonCommercial-No Derivative Works 4.0 International License.

Recommended Citation

Katt, Taylor E.; Spicer, Robert L.; Yetman, Anji T.; Ibrahimiye, Ali N.; Hammel, James M.; and Robinson, Jeffrey A., "Williams Syndrome and Neonatal Cardiac Surgery for Congenital Single Ventricle" (2020). Journal Articles: Pediatrics. 34.
https://digitalcommons.unmc.edu/com_peds_articles/34