Results 1 to 10 of about 1,817,418 (245)

Aortic Arch Anomalies and Pulmonary Artery Anomalies : Echocardiographic Evaluation

open access: yesJournal of the Indian Academy of Echocardiography & Cardiovascular Imaging, 2020
Congenital variants and anomalies of the aortic arch are important to recognize as they may be associated with vascular rings, congenital heart disease, and chromosomal abnormalities, and can have important implications for prognosis and management.
Prashant Mahawar
doaj   +2 more sources

Double aortic arch [PDF]

open access: yesNetherlands Heart Journal, 2007
A 58-year-old male was referred to our outpatient cardiology clinic for evaluation of atrial fibrillation, fatigue, dizziness and exertional dyspnoea. He had suffered recurrent pneumonia in childhood. Beside an irregular pulse, the physical examination was normal.
Nijveldt, R.   +4 more
openaire   +4 more sources

Study on the views and methods of ultrasonic screening and diagnosis for abnormal aortic arch in infants

open access: yesCardiovascular Ultrasound, 2021
Background The purpose of this study was to explore echocardiographic views and methods of aortic arch anomalies in infants, so as to improve the screening sensitivity and diagnostic accuracy.
Xinjian He, Jiaoyang Chen, Gaoyang Li
doaj   +1 more source

Co-dominant vascular ring in a blue baby causing dysphagia – A rare occurrence

open access: yesIHJ Cardiovascular Case Reports, 2020
Double aortic arch is a rare form of congenital cardiac malformation causing respiratory and esophageal symptoms. We present a rare case of co-dominant Double aortic arch with tetralogy of Fallot which was successfully treated.
Chandrasekaran Ananthanarayanan   +3 more
doaj   +1 more source

Pseudoaneurysm Complicating Anterior Arch of Congenital Double Aortic Arch

open access: yesActa Medica Iranica, 2020
Aortic rupture and pseudoaneurysm formation in the anterior arch of congenital double aortic arch anomaly associated with a coarctation is an exceedingly rare complication of aortic vascular ring.
Atefeh Asadmobini   +2 more
doaj   +1 more source

Double aortic arch in an adult [PDF]

open access: yesInteractive CardioVascular and Thoracic Surgery, 2012
We present the case of a 60-year old man who complained of severe dysphagia caused by a double aortic arch (DAA) with a right-sided descending thoracic aorta. The left-sided aortic arch had a compressive segment located between the left subclavian artery and the descending thoracic aorta.
Kenichiro, Noguchi   +3 more
openaire   +2 more sources

Right upper lobectomy in lung cancer with double aortic arch: A case report

open access: yesThoracic Cancer, 2020
Double aortic arch (DAA) is a rare congenital anomaly of the heart and aorta in which a vascular ring that surrounds the trachea and esophagus is formed.
Nobutaka Kawamoto   +6 more
doaj   +1 more source

A new association of Oculoauriculovertebral spectrum and persistent fifth aortic arch -double lumen aorta: a case report

open access: yesBMC Pediatrics, 2022
Background Oculo-auriculo-vertebral spectrum is a heterogeneous group of genetic disorder, also known as Goldenhar Syndrome, which has several phenotypic features including craniofacial anomalies, cardiac, vertebral and central nervous system defects ...
İsmail Balaban   +2 more
doaj   +1 more source

Double-Lumen Aortic Arch: Persistence of the Fifth Aortic Arch [PDF]

open access: yesThe Annals of Thoracic Surgery, 2016
A persistent fifth aortic arch is exceptionally rare. We report a patient with a double-lumen aortic arch in association with a perimembranous ventricular septal defect and Cornelia de Lange syndrome. We also discuss the morphologic consequences of persistent fifth aortic, arch, which may not be limited to the double-lumen aorta but in fact may be more
Phillip S, Naimo   +4 more
openaire   +2 more sources

Right aortic arch with mirror image branching pattern and isolated left brachiocephalic artery: A case report

open access: yesRadiology Case Reports, 2020
We present a very rare case of right aortic arch with an isolated left brachiocephalic artery in a 35-year-old female. This entity is an extremely uncommon aortic arch anomaly which has associated multisystem symptoms. We briefly discuss the hypothetical
Ayman Nada, MD, PhD   +3 more
doaj   +1 more source

Home - About - Disclaimer - Privacy