Year: 2011
Type: article
Abstract: *Corresponding author. E-mail address: [email protected] (F. Silva). Right aortic arch is a cardiovascular malformation or a variant of normality which can be diagnosed by prenatal ultrasound. This malformation may be associated with DiGeorge syndrome (arising from defects in chromosome 22) and can result in posterior compression of the trachea and esophagus, leading to dysphagia and respiratory impairment after birth. Figure A Right aortic arch passing posterior to the trachea. AO: aorta; PA: pulmonary artery; RV: right ventricle; SVC: superior vena cava; TR: trachea.
Authors: Fátima Silva, Cristina Godinho, Ana Carriço
Institution: Centro Hospitalar de Vila Nova de Gaia
Language: English
Subfield: Cardiology and Cardiovascular Medicine
Field: Medicine
Domain: Health Sciences
Open Access status: diamond
OpenAlex ID: W2098568351
