Results 71 to 80 of about 49,151 (247)

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

open access: yesMedical 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   +3 more
doaj   +1 more source

Double Aortic Arch Surgery

open access: yesIndian Journal of Vascular and Endovascular Surgery, 2015
A 4-year-old male child was admitted with a history of difficulty in swallowing, failure to thrive and recurrent respiratory tract infections. On investigations, cardiac computed tomography was suggestive of a double aortic arch (DAA) and a virtual bronchoscopy was suggestive of tracheomalacia.
Dwarkanath V Kulkarni   +1 more
openaire   +2 more sources

Double Aortic Arch with Coarctation of Aorta in an Adolescent: Unraveling the Vascular Ring

open access: yesAorta, 2020
We report the case of a 12-year-old girl with balanced double aortic arch with coarctation of the aorta presenting with symptoms of respiratory and swallowing difficulty.
Bijoy G Rajbanshi   +8 more
semanticscholar   +1 more source

A Soft‐Tip Hydraulically Steerable Catheter for Enhanced Flexibility and Safety in Vascular Interventions

open access: yesAdvanced Intelligent Systems, EarlyView.
This study introduces a hydraulically steerable catheter with a soft tip in vascular procedures. The steering soft tip achieves a minimal diameter of 2.6 mm and supports a 180° bend. Real‐time shape and position tracking, facilitated by segmentation and endpoint detection techniques, improves navigation.
Jingyi Kang   +9 more
wiley   +1 more source

The Prevalence of Aortic Arch Anomalies in Children Who Underwent Cardiac Catheterization: A Single-center Experience

open access: yesJournal of Behçet Uz Children's Hospital, 2019
INTRODUCTION: We aimed to determine the prevalence of aortic arch anomalies in children who underwent cardiac catheterization and angiography for various reasons.
Ferit Kulalı   +5 more
doaj   +1 more source

DOUBLE AORTIC ARCH - A CASE REPORT912

open access: yesPakistan Armed Forces Medical Journal, 2020
Double Aortic Arch is a rare congenital cardiovascular anomaly. Its first successful surgery was performed by Robert Gross in 1945 at Children Hospital Boston, USA. It accounts for 0.4 to 1% of all congenital cardiac defects.
Syed Shahid Nafees   +3 more
doaj   +1 more source

Artificial Intelligence Software Changes Rare Disease Testing Strategy in Real Time: An International Case Series Using Face2Gene

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Genetic disorders commonly share features such as developmental delays, cognitive impairment, and behavioral challenges, yet many conditions also present unique dysmorphic features that distinguish them. Performing a thorough medical and family history and a detailed physical exam with attention to dysmorphic features is often the first step ...
Natasha L. Rudy   +15 more
wiley   +1 more source

Incidental finding of double aortic arch and tract from noncoronary sinus to left atrium: A case report

open access: yesRadiology Case Reports
The double aortic arch with vascular ring is a rare but documented aortic arch variant, traditionally presenting with difficulty swallowing or breathing due to extrinsic compression.
Jin Kai Soh, MBChB   +2 more
doaj   +1 more source

Experience of diagnosis of congenital arterial anomaly in a child with bronchial obstruction: clinical case and summary

open access: yesZdorovʹe Rebenka, 2017
Congenital anomalies of the aortic arch are a large group of cardiovascular anomalies. Some of them are isolated; others are associated with congenital heart defects or genetic syndromes. There can be different clinical manifestations of these anomalies —
L.V. Besh   +8 more
doaj   +1 more source

Trisomy 5p: Long Recognized, Rarely Published‐ Three New Cases and Review of the Literature

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Complete trisomy 5p is a rare chromosomal disorder caused by a duplication of the short arm of chromosome 5. Current data suggest that complete trisomy 5p presents as a distinct clinical syndrome including but not limited to seizures, developmental delays, facial dysmorphisms, failure to thrive, and recurrent respiratory infections.
Gabriela J. Kim   +2 more
wiley   +1 more source

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