Results 21 to 30 of about 11,540 (186)

Assessment of CT angiographic findings in comparison with echocardiography findings of chest among patients with aortic arch anomalies

Monaldi Archives for Chest Disease, 2019
The objective of this study was to examine the findings of computed tomographic (CT) angiography in patients with aortic arch anomalies in comparison with transthoracic echocardiography findings who referred to a private imaging center in Tehran during ...
Hussein Soleimantabar, Sofia Sabouri, Leila Khedmat, Samira Salajeghe, Behzad Memari, Bahareh Heshmat Ghahderijani   +5 more
doaj   +1 more source

Combined Anatomical Anomalies of Direct Aortic Arch Origins of the Left Internal Carotid, Left External Carotid, and Left Vertebral Arteries: A Case Report

Journal of the Korean Society of Radiology, 2023
Various branch anomalies of the aortic arch have been reported, but cases with separate origins of the internal and external carotid arteries with combined direct aortic arch origin of the left vertebral artery are extremely rare.
Dae Yun Park, Byunghoon Lee, Yoon Joon Hwang   +2 more
doaj   +1 more source

An unusual case of unilateral vascular hypoplasia in an adult patient – late diagnosis of PHACE syndrome

International Journal of Cardiology Congenital Heart Disease, 2023
A case of unilateral vascular hypoplasia is presented. A female patient was born with a complex aortic arch anatomy - a double aortic arch with an interrupted left arch. Surgical correction was performed at the age of 3 months. The patient was also noted
Madelien V. Regeer, J. Lauran Stöger, Regina Bökenkamp, Inge M.M. Lakeman, Mark G. Hazekamp, Philippine Kiѐs, Anastasia D. Egorova, Monique R.M. Jongbloed   +7 more
doaj   +1 more source

Persistent Fifth Aortic Arch Associated with 22q11.2 Deletion Syndrome

Journal of the Formosan Medical Association, 2006
Chromosome 22q11.2 deletion is frequently associated with conotruncal malformations and aortic arch anomalies. This study investigated the association of chromosome 22q11.2 deletion with clinical manifestations in four pediatric patients with persistent ...
Meng-Luen Lee
doaj   +1 more source

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

Cardiovascular 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

Imaging findings in the right aortic arch with mirror image branching of arch vessels: An unusual cause of dysphagia

Medical Journal of Dr. D.Y. Patil University, 2015
We report a case of a 72-year-old female with a right aortic arch with mirror-image branching of arch vessels presenting with dysphagia, and characteristic images on barium esophagogram, contrast-enhanced computed tomography scan, and magnetic resonance ...
Guneet Singh, Amit Kharat, Preeti Sehrawat, Vilas Kulkarni   +3 more
doaj   +1 more source

Congenital Variants and Anomalies of the Aortic Arch [PDF]

RadioGraphics, 2017
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. The purpose of this article is to review cross-sectional imaging techniques used in the evaluation of ...
Kate, Hanneman, Beverley, Newman, Frandics, Chan   +2 more
openaire   +2 more sources

Right aortic arch with common origin of right carotid and left innominate artery: A case report

Clinical Case Reports, 2022
Aortic arch anomalies are rare congenital malformations with an incidence of approximately 1–3%. Right aortic arch is an anatomical variant with an incidence of
Swati Chand, Omofolarin Babayale, Devesh Rai, Sangharsha Thapa, Sangam Shah, Jeremiah P. Depta, Bipul Baibhav   +6 more
doaj   +1 more source

Aberrant Right Subclavian Artery: Cadaver Case Report

International Journal of Medical Students, 2023
While examining the anatomy of a cadaver in a medical school gross anatomy course, an aortic arch anomaly was discovered. This variant is consistent with an aberrant right subclavian artery (ARSA).
Jason Kopp, Ahmad Irshaid, Justin Baker, John Fitzsimmons, Judith C. Lin   +4 more
doaj   +1 more source

ADNP‐Related Helsmoortel–Van der Aa Syndrome: A Review of the Literature and Clinical Recommendations for Assessment and Monitoring

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT ADNP‐related Helsmoortel–Van der Aa syndrome (ADNP‐related HVDAS) is a single gene form of autism spectrum disorder (ASD) caused by pathogenic sequence variants in the activity‐dependent neuroprotective protein (ADNP) gene. In addition to ASD, ADNP‐related HVDAS is associated with a wide range of cognitive, behavioral, and physical health ...
Jarrett Fastman, Ana Kolevzon, Paige Siper, Tess Levy, Jeffrey M. Saland, Yitzchak Frank, Robert Rapaport, Kayla Kupietzky, William E. Bennett Jr, Bruce Gelb, Sandra Bedrosian Sermone, Alexander Kolevzon   +11 more
wiley   +1 more source