Results 61 to 70 of about 2,957,223 (168)
American Journal of Medical Genetics Part C: Seminars in Medical Genetics, Volume 199, Issue 2, Page 51-71, June 2025.ABSTRACT Turner syndrome (TS) is frequently complicated by congenital heart disease (CHD). While left‐sided lesions such as bicuspid aortic valve (BAV) and coarctation of the aorta are the most common structural heart lesions in TS, other anomalies, such as aortic arch malformations, hypoplastic left heart syndrome (HLHS), persistent left superior vena
Katya de Groote +9 more
wiley +1 more source
A rare cause of dysphagia--aberrant right subclavian artery (ARSA).
European review for medical and pharmacological sciences, 2009 Aberrant Right Subclavian Artery (ARSA) is a rare vascular anomaly. It is though the most frequent anomaly involving the aortic arch, being present in about 1% of the general population. We present a case of a 71 year old male with symptoms of chronic cough and dysphagia. He was referred to our clinic for further evaluation of a mediastinal mass.
V, Tzilas, A, Koti, G, Tsoukalas
openaire +1 more source
Strategies to Detect Chromosomal Anomalies Not Identified by NIPT
Prenatal Diagnosis, Volume 45, Issue 4, Page 464-472, April 2025.ABSTRACT Introduction Genome‐wide non‐invasive prenatal testing (gwNIPT) has screening limitations for detectable chromosomal conditions and cannot detect microdeletions/microduplications (MD) or triploidy. Thickened nuchal translucency (NT) only detects around 10% of these cases. Methods A 4‐year retrospective study of singleton pregnancies undergoing
Fergus Scott +4 more
wiley +1 more source
CJC Pediatric &Congenital Heart Disease, Volume 4, Issue 2, Page 55-60, April 2025.Abstract Background Vascular rings and slings are the most common aortic arch anomalies. The age of presentation and diagnosis is typically 0‐6 months. Diagnostic methods have shifted with increasing preference for echocardiograms related to technique, quality, and understanding. Therefore, we aimed to examine the rising prevalence of vascular ring and
Mark D. Bertone +3 more
wiley +1 more source
Simultaneous hybrid treatment of aneurysmal aberrant right subclavian artery
, 2015 We review the literature and report our experience on the simultaneous hybrid treatment (open and endovascular) of two symptomatic aneurysms of an aberrant right subclavian artery (ARSA). At follow-up (four years and one year, respectively) both patients
Chisci E. +4 more
core +1 more source
Three concurrent variations of the aberrant right subclavian artery, the non-recurrent laryngeal nerve and the right thoracic duct [PDF]
, 2016 We herein report a case showing three anatomical variations including the aberrant right subclavian artery (ARSA), the non-recurrent laryngeal nerve (NRLN) and the right thoracic duct in a 59-year-old male cadaver. The right subclavian artery (RSA) arose
Lee, J.-Y.; Department of Anatomy and Neuroscience, Eulji University School of Medicine, Daejeon, Republic of Korea +7 more
core +1 more source
Veterinary Radiology &Ultrasound, Volume 66, Issue 2, March 2025.ABSTRACT Aberrant right subclavian arteries (ARSAs) are a form of vascular ring anomaly (VRA) in dogs and the most common VRA in people. To date, there has been no large‐scale study on ARSA in dogs and their potential clinical significance. For part one, a single‐center retrospective observational study was performed to determine the prevalence of ...
Coleen Jones +5 more
wiley +1 more source
Clinical Case Reports, Volume 13, Issue 1, January 2025.ABSTRACT Four‐dimensional flow magnetic resonance imaging (4D flow MRI) was utilized to analyze an aortic dissection with an aberrant right subclavian artery, revealing vortex formation and an increased oscillatory shear index (OSI), both indicative of variations in wall shear stress.
Kenji Sakakibara +12 more
wiley +1 more source
SAGE Open Medical Case Reports, 2022 An aberrant right subclavian artery (ARSA) is an extremely rare congenital anomaly that forms during aortic arch development. Most reports of thoracic endovascular aortic repair (TEVAR) described an ARSA in the right aortic arch, but it is rare in the ...
Yasuhito Nakamura +5 more
doaj +1 more source
Prenatal cardiac findings and 22q11.2 deletion syndrome: Fetal detection and evaluation
Prenatal Diagnosis, Volume 44, Issue 6-7, Page 804-814, June 2024.Abstract Clinical features of 22q11.2 microdeletion syndrome (22q11.2DS) are highly variable between affected individuals and frequently include a subset of conotruncal and aortic arch anomalies. Many are diagnosed with 22q11.2DS when they present as a fetus, newborn or infant with characteristic cardiac findings and subsequently undergo genetic ...
Elizabeth Goldmuntz +10 more
wiley +1 more source