Results 61 to 70 of about 308 (124)

An uncommon cardiovascular abnormality: Case report of core triatriatum associated with persistent left superior vena cava and coronary sinus dilation

open access: yesRadiology Case Reports
Cor triatriatum is an uncommon cardiac defect that occurs in 0.1-0.4% of congenital heart disease patients. It is characterized by a fibromuscular membrane separating the left (sinister) or the right (Dexter) atriums in tow chambers.
Yunis Daralammouri, MD   +2 more
doaj   +1 more source

Incidental discovery of an unusual right atrial membrane in an adult patient

open access: yesAnnals of Cardiac Anaesthesia, 2012
We describe presence of an unusual right atrial membrane in a 30-year old female with end stage renal disease, hypertension and peripheral vascular disease.
Nasrin N Aldawoodi   +2 more
doaj   +1 more source

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   +2 more sources

Successful surgical correction of symptomatic cor triatriatum dexter

open access: yesThe Journal of Thoracic and Cardiovascular Surgery, 1979
An unusual case of cor triatriatum dexter is presented. Abnormal embryologic development of the eustachian valve caused nearly complete septation of the right atrium in a 67-year-old woman. Multiple supraventricular arrhythmias prompted clinical evaluation and diagnosis.
D A, Ott   +3 more
openaire   +2 more sources

Successful repair of symptomatic cor triatriatum dexter in infancy

open access: yesThe Journal of Thoracic and Cardiovascular Surgery, 1983
Cor triatriatum dexter is a rare cardiac malformation, usually diagnosed incidentally at operation or necropsy. We report the case of a 5-month-old infant, severely symptomatic, who underwent correction of a highly obstructive cor triatriatum dexter, with multiple anomalies of the systemic venous return and a large interatrial communication.
MAZZUCCO, Alessandro   +4 more
openaire   +3 more sources

[Echocardiography in cor triatriatum dexter].

open access: yesRevista portuguesa de cardiologia : orgao oficial da Sociedade Portuguesa de Cardiologia = Portuguese journal of cardiology : an official journal of the Portuguese Society of Cardiology, 1994
"Cor triatriatum dexter" (CTD) is an unusual cyanotic cardiac defect in which the right atrium is subdivided into two distinct chambers due to the persistence of the "sinus venosus" valve. Two patients with CTD ho were evaluated and treatment in 1979 and 1992 are described: the first one, had total anomalous pulmonary venous return to the coronary ...
M A, Nunes, J, Fragata, M, Lima
openaire   +1 more source

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   +2 more sources

COR TRIATRIATUM DEXTER

open access: yesJournal of Evolution of Medical and Dental Sciences, 2015
Debasish Das, Satyabrata Guru
openaire   +1 more source

Cor triatriatum dexter in adults: Clinical implications [PDF]

open access: yesThe Journal of Thoracic and Cardiovascular Surgery, 2016
Syed T, Hussain, Gösta B, Pettersson
openaire   +2 more sources

Ecocardiografia em «Cor Triatriatum Dexter»

open access: yes, 1993
"Cor triatriatum dexter" (CTD) is an unusual cyanotic cardiac defect in which the right atrium is subdivided into two distinct chambers due to the persistence of the "sinus venosus" valve. Two patients with CTD ho were evaluated and treatment in 1979 and 1992 are described: the first one, had total anomalous pulmonary venous return to the coronary ...
Nunes, MA, Fragata, J, Lima, M
openaire   +1 more source

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