Results 11 to 20 of about 446 (142)

Partial Venous Inflow Occlusion under Mild Hypothermia for Membranectomy in a Dog with Cor Triatriatum Dexter

open access: yesAnimals, 2023
Cor triatriatum dexter (CTD) is an uncommon congenital cardiac anomaly in dogs. This case report describes successful membranectomy for CTD via partial venous inflow occlusion under mild hypothermia in a dog.
Chang-Hwan Moon   +8 more
doaj   +3 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 Mimicking Ebstein Disease [PDF]

open access: yesCirculation, 2009
A 4-month-old girl was referred for cyanosis and echocardiographic suspicion of Ebstein anomaly. Medical history had been uneventful thus far. At clinical examination, she was restless and cyanosed but did not show respiratory distress, cardiac failure, or failure to thrive.
C. Barrea   +3 more
openaire   +3 more sources

Cor Triatriatum Dexter in a Male Cadaver [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2018
Cor Triatriatum Dexter (CTD), is a very rare congenital anomaly in which right atrium is partitioned to form three chambered heart. It is caused by the persistence of the right valve of the sinus venosus.
Pooja Bhadoria, Neelam Vasudeva
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 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

Multimodality imaging of cor triatriatum dexter complicated with hypertrophic cardiomyopathy of restrictive phenotype

open access: yesRadiology Case Reports, 2022
Cor triatriatum dexter (CTD) is an extremely rare congenital cardiac malformation in which a membrane divides the right atrium into 2 chambers. Hypertrophic cardiomyopathy (HCM) with restrictive phenotype is also a rare cardiomyopathy.
Li Liang, Min-Jie Lu, PhD
doaj   +3 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 with imperforate Ebstein's anomaly. [PDF]

open access: yesHeart, 1976
A case of cor triatriatum dexter is described in which the anomalous right atrial partition is identified as the right venous valve; there is an associated anomaly of the right atrioventricular valve which combines features of Ebstein's anomaly, and an atypical, imperforate, tricuspid atresia.
L M, Gerlis, R H, Anderson
openaire   +4 more sources

Cor triatriatum dexter: Two-dimensional echocardiography diagnosis

open access: yesJournal of the American College of Cardiology, 1987
Cor triatriatum dexter is a malformation resulting from lack of normal regression of the embryonic right valve of the sinus venosus. In this situation, the right atrium is divided by a membrane into two chambers. Two-dimensional echocardiography was used in the antemortem diagnosis of this rare cardiac anomaly in a neonate.
Alboliras, Ernerio T.   +3 more
openaire   +4 more sources

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