Results 21 to 30 of about 18,091 (144)

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

A rare case of symptomatic vascular ring

open access: yesRadiology Case Reports, 2023
In this paper, we describe a rare case of double aortic arch with dominant right arch with focal narrowing of the distal left arch and descendent aorta's dilatation, associated with pulmonary embolism and left subclavian steal syndrome, found in a 59 ...
Marcello Chiocchi, PhD   +6 more
doaj   +1 more source

A rare association with patent ductus arteriosus

open access: yesAnnals of Pediatric Cardiology, 2012
Persistent fifth aortic arch (PFAA), also known as congenital double-lumen aortic arch, is a rare developmental anomaly of the aortic arch. A 5-month-old baby who presented with congestive cardiac failure was diagnosed to have a large patent ductus ...
Dhanya Warrier   +3 more
doaj   +1 more source

[Double aortic arch]. [PDF]

open access: yesVestnik khirurgii imeni I. I. Grekova, 2000
A7-year-old girl presented with severe dyspnea and pneumonia, which required endotracheal intubation, mechanical ventilation, and intravenous antibiotics. She had a history of several severe airway infections with inspiratory stridor. After she recovered, a bronchoscopy and an esophagogram (Figure 1⇓) were performed to screen for a vascular ring.
A P, KOLESOV, F Kh, KUTUSHEV
openaire   +3 more sources

Case report and literature review: fetal diagnosis of vascular ring with circumflex right aortic arch and unique aortic arch branching pattern

open access: yesFrontiers in Cardiovascular Medicine
Circumflex right aortic arch is a rare aortic arch anomaly where the arch extends in a retro-esophageal pattern with a left-sided descending thoracic aorta.
Tyler Langenfeld   +3 more
doaj   +1 more source

Double symmetrical aortic arch in a Czechoslovakian wolfdog - surgical treatment and health assessment four years after treatment: a case report

open access: yesVeterinární Medicína, 2017
The paper describes a double symmetrical aortic arch in a dog trapping the oesophagus. Thoracotomy was performed in the fourth inter-costal space under general, isoflurane-maintained, anaesthesia.
P. Skrzypczak   +3 more
doaj   +1 more source

Recurrent Wheezing and Cough Caused by Double Aortic Arch, Not Asthma

open access: yesCase Reports in Cardiology, 2017
Introduction. Double aortic arch is a congenital vascular abnormality in which the connected segments and their branches course between and compress the trachea and esophagus, often resulting in invariable airway compression. Case Presentation.
Qiao Zhang   +5 more
doaj   +1 more source

Right aortic arch with isolation of the left innominate artery in a case of double chamber right ventricle and ventricular septal defect

open access: yesAnnals of Pediatric Cardiology, 2014
Herein, we report an unusual case of right aortic arch with isolation of the left innominate artery in a case of double chamber right ventricle with ventricular septal defect. The blood supply to the innominate artery was by a collateral arising from the
Chirantan Mangukia   +4 more
doaj   +1 more source

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