Results 31 to 40 of about 1,817,418 (245)

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: yesActa chirurgica Scandinavica, 2004
54-year-old woman presented with a 1-year history of a full sensation in the throat and an 8-month history of dysphagia with meat and large pills. She was treated for gastroesophageal reflux disease without relief. An esophagram revealed mild compression of the cervical esophagus.
G, EKSTROM, P, SANDBLOM
  +6 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

Surgical Repair of Double Aortic Arch Through Sternotomy

open access: yes, 2023
This video illustrates surgical repair of double aortic arch through a sternotomy. Double aortic arch is the most common type of vascular ring malformation. It involves complete encirclement of the trachea and esophagus by the aortic arch or its branches.
Servet Ergün (7031657)   +3 more
core   +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

Prenatal aortic arch development in double aortic arch: Understanding postnatal closure of left aortic arch: A case report. [PDF]

open access: yesRadiol Case Rep
Double aortic arch (DAA) is a rare congenital abnormality characterized by a vascular ring that often requires surgical intervention due to respiratory complications.
Isohata H   +11 more
europepmc   +2 more sources

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

Total Endovascular Aortic Arch Repair: From Dream to Reality

open access: yesMedicina, 2022
The gold-standard therapy for the treatment of aortic arch pathologies is conventional open surgery. Recently, total endovascular aortic arch replacement with branched stent-grafts has been introduced into clinical practice with the aim of reducing ...
Augusto D’Onofrio   +4 more
doaj   +1 more source

ZER1 Restrains Pressure Overload‐Induced Cardiac Remodeling by Targeting DVL2 for Gly/N‐Degron‐Dependent Degradation

open access: yesAdvanced Science, EarlyView.
Pressure overload suppresses cardiomyocyte ZER1, weakening CRL2Zer1‐mediated DVL2 degradation and allowing DVL2 accumulation. Elevated DVL2 activates CaMKII‐HDAC4‐MEF2C signaling, drives fetal gene reactivation, and promotes pathological remodeling.
Mingchao Jiang   +27 more
wiley   +1 more source

Dysphagia in an adult tetralogy of fallot with double aortic arch [PDF]

open access: yes, 2013
Double aortic arch (DAA) is a common vascular ring. It may occur in isolation or coexist with various types of congenital heart disease . The anomaly usually presents in early infancy.
Bhan, Anil   +2 more
core  

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