Improved Outcomes in Patients with 22q11.2 Deletion Syndrome and Diagnosis of Interrupted Aortic Arch Prior to Birth Hospital Discharge, a Retrospective Study

Improved Outcomes in Patients with 22q11.2 Deletion Syndrome and Diagnosis of Interrupted Aortic Arch Prior to Birth Hospital Discharge, a Retrospective Study

Interruption of the aortic arch (IAA) is a rare but life-threatening congenital heart defect if not corrected in the neonatal period. IAA type B is highly correlated with 22q11.2 deletion syndrome (22q11.2DS); approximately 50% of patients with IAA type B also have 22q11.2DS (Peyvandi et al.; Goldmu...

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Bibliographic Details
Main Authors: Hayley A. Ron, Terrence Blaine Crowley, Yichuan Liu, Marta Unolt, Erica Schindewolf, Julie Moldenhauer, Jack Rychik, Elizabeth Goldmuntz, Beverly S. Emanuel, Douglas Ryba, James William Gaynor, Elaine H. Zackai, Hakon Hakonarson, Donna M. McDonald-McGinn
Format: Article
Language:English
Published: MDPI AG 2022-12-01
Series:Genes
Subjects:
interrupted aortic arch
type B interrupted aortic arch
22q11.2 deletion syndrome
congenital heart disease
critical congenital heart disease screening
prenatal diagnosis
Online Access:https://www.mdpi.com/2073-4425/14/1/62

Internet

https://www.mdpi.com/2073-4425/14/1/62

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