Author + information
- Received March 20, 2020
- Revision received May 6, 2020
- Accepted May 20, 2020
- Published online September 16, 2020.
- Taylor E. Katt, MDa,
- Robert L. Spicer, MDb,c,
- Anji T. Yetman, MDb,c,
- Ali N. Ibrahimiye, MDb,d,
- James M. Hammel, MDb,d and
- Jeffrey A. Robinson, MDb,c,∗ ()
- aCollege of Medicine, University of Nebraska Medical Center, Omaha, Nebraska
- bDr. C.C. and Mabel L. Criss Heart Center, Children’s Hospital and Medical Center, Omaha, Nebraska
- cDepartment of Pediatrics, Division of Cardiology, College of Medicine, University of Nebraska Medical Center, Omaha, Nebraska
- dDepartment of Surgery, College of Medicine, University of Nebraska Medical Center, Omaha, Nebraska
- ↵∗Address for correspondence:
Dr. Jeffrey A. Robinson, Pediatric Cardiology, Dr. C.C. and Mabel L. Criss Heart Center, Children's Hospital & Medical Center, 8200 Dodge Street, Omaha, Nebraska 68114-4113.
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.)
The authors have reported that they have no relationships relevant to the contents of this paper to disclose.
The authors attest they are in compliance with human studies committees and animal welfare regulations of the authors’ institutions and Food and Drug Administration guidelines, including patient consent where appropriate. For more information, visit the JACC: Case Reports author instructions page.
- Received March 20, 2020.
- Revision received May 6, 2020.
- Accepted May 20, 2020.
- 2020 The Authors