Results 21 to 30 of about 308 (124)

Cor Triatriatum Dexter: The Largest Comprehensive Review in the Field on 124 Worldwide Cases (1968–Now) [PDF]

open access: yesJournal of Cardiovascular Development and Disease
Background. Cor triatriatum dexter (CTD) is a rare congenital heart defect where a membrane divides the right atrium into two chambers, resulting from the incomplete regression of the right valve of the sinus venosus.
Pier Paolo Bassareo   +7 more
doaj   +2 more sources

Presumed atypical cor triatriatum dexter in a geriatric dog: A case report [PDF]

open access: yesVeterinární Medicína
Membranous structures within the right atrium (RA), such as the Chiari network, eustachian valve, Thebesian valve, and cor triatriatum dexter (CTD), can present with overlapping imaging features and complicated diagnoses.
Y Jeong, D Kwon, K Park, K Lee, H Yoon
doaj   +2 more sources

A Rare Complication During Transcatheter Closure of Double Atrial Septal Defects With Incomplete Cor Triatriatum Dexter: A Case Report [PDF]

open access: yesFrontiers in Cardiovascular Medicine, 2022
The cor triatiatum dexter is an embryologic remnant derived from the right atrium and totally separate from the right atrium. An incomplete cor triatiatum dexter (iCTD) means a partially obstructive remnant at the right atrium.
Ping-Hong Chen   +11 more
doaj   +2 more sources

COR TRIATRIATUM DEXTER EN LA EDAD ADULTA / Cor triatriatum dexter in adulthood [PDF]

open access: yesCorSalud, 2013
Resumen: El cor triatriatum dexter es una malformación muy rara, en el cual la aurícula derecha está dividida en dos cámaras por un tabique. Se presenta el caso de una joven de 24 años de edad con antecedentes de insuficiencia cardíaca por miocardiopatía
Aliet Arrué Guerrero   +2 more
doaj   +1 more source

Cor triatriatum dexter with pulmonary hypertension

open access: yesSahel Medical Journal, 2016
Cor triatriatum (CT) otherwise known as a tri atrial heart is a rare congenital heart defect. This report describes a rare case of CT dexter in a 2-year-old girl who presented to our facility with cough and difficulty in breathing of a year duration and ...
O Mustafa Asani   +2 more
doaj   +2 more sources

A Rare Case: Cor Triatriatum Dexter

open access: yesSouthern Clinics of Istanbul Eurasia, 2017
Cor triatriatum dexter (CTD) is a rare congenital heart disorder that is result of persistence of the right valve of the embryonic sinus venosus. Clinical significance of CTD is related to degree of obstruction.
Ali Orgun   +4 more
doaj   +2 more sources

Cor triatriatum dexter in Dogs: A Silent Bystander or a Potential Time Bomb? A Focused Literature Review from a Professional Perspective [PDF]

open access: yesVeterinary Sciences
Congenital heart diseases (CHDs) are structural anomalies present at birth, resulting from aberrant embryonic development. In veterinary medicine, CHDs are an important reason for disease and death in both dogs and cats.
Michela Pugliese   +6 more
doaj   +2 more sources

Clinical case of Cor triatriatum sinister, a dilemma of anticoagulation: A case report and literature review

open access: yesClinical Case Reports
Key Clinical Message Cor triatriatum is a rare congenital heart abnormality in which a membrane separates the left atrium (LA; sinister) or the right atrium (dexter) into two compartments. It is also a long‐forgotten cause of atrial fibrillation (AF) and
Alireza Arzhangzade   +6 more
doaj   +2 more sources

Cor triatriatum dexter: A rare cause of childhood cyanosis

open access: yesAnnals of Pediatric Cardiology, 2012
Cor triatriatum dexter is a rare congenital heart anomaly where the right atrium is divided into two chambers by a membrane. We report a boy who had persistent mild cyanosis and diagnosed to have cor triatriatum dexter with secundum atrial septal defect ...
Ahmad Rustam bin Mohd Zainudin   +2 more
doaj   +3 more sources

Cor triatriatum dexter: A rare cause of cyanosis during neonatal period

open access: yesAnnals of Pediatric Cardiology, 2016
Cor-triatriatum dexter is an extremely rare congenital heart defect in which there is complete persistence of the right valve of embryonic sinus venosus that results in partitioning of the right atrium into a smooth and trabeculated portion.
Mohammed Hussien Alghamdi
doaj   +2 more sources

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