Results 41 to 50 of about 2,799 (206)

Transcatheter Closure of Atrial Septal Defect in a Patient with Cor Triatriatum Sinister and Atrial Septal Defect

Case Reports in Cardiology, 2011
Cor triatriatum sinister is a rare congenital heart disease and rarely found in adults. The authors describe an asymptomatic 20-year old man presenting with heart murmur by check up.
Wasana Hongkan, Kriangsak Thongchaiprasit, Kritvikrom Durongpisitkul   +2 more
doaj   +1 more source

Right Atrial Aneurysm after Chest Trauma: Late Presentation [PDF]

, 2012
Relata-se o caso de um paciente de 59 anos de idade, com história de traumatismo torácico grave com fratura de vários arcos costais aos 20 anos, com início recente de cansaço e palpitações, a quem foi detetada taquicardia auricular, convertida ...
Branco, LM, Cota, C, Cruz Ferreira, R, Galrinho, A, Santos, N, Silva Cunha, P, Sousa, L, Timóteo, AT   +7 more
core   +1 more source

ISOLATED COR TRIATRIATUM SINISTER : A CASE REPORT [PDF]

, 2020
Cor triatriatum sinister is a rare congenital cardiac anomaly that has been identified in 0.1% of children with congenital heart disease. It is defined as a fibromuscular membrane that divides the left atrium into two chambers: a superior (proximal) that
Auziņa, Luīze, Bergmane, Inta, Grīnberga, Zanda, Ligere, Elina, Lubaua, Ingūna, Lāce, Inga, Ozolins, Valts, Sikora, Normunds, Smits, Lauris, Sīlis, Pauls   +9 more
core   +1 more source

A Case of Acquired Cor Triatriatum Dextrum

Journal of the Indian Academy of Echocardiography & Cardiovascular Imaging
Cor triatriatum is a rare congenital heart condition, with cor triatriatum sinistrum being more common than cor triatriatum dextrum. Most patients are asymptomatic, but some may experience symptoms due to inflow obstruction.
M. Haashim, M. Nandakumaran, G. Prathap Kumar, D. Rajasekhar Ramesh   +3 more
doaj   +1 more source

A paediatric telecardiology service for district hospitals in south-east England: an observational study. [PDF]

, 2008
The attached article is a Publisher version of the final published version which may be accessed at the link below. Copyright © 2010 BMJ Publishing Group Ltd & Royal College of Paediatrics and Child Health.
Dowie, R, Franklin, RC, Mistry, H, Rigby, M, Rowlinson, G, Weatherburn, G, Young, TA   +6 more
core   +2 more sources

Successful implantation of a biventricular pacing and defibrillator device via a persistent left superior vena cava [PDF]

, 2013
Introduction. Persistent left superior vena cava is the most common thoracic venous abnormality which is usually asymptomatic, found incidentally during pacemaker implantation.
Angelkov Lazar, Tomašević-Vukmirović Irena, Vukmirović Filip, Vukmirović Mihailo   +3 more
core   +1 more source

A six-chambered heart: cor triatriatum sinister with double-chambered right ventricle in association with ventricular septal defect

The Egyptian Heart Journal, 2022
Background Cor triatriatum has been described as a heart with three atria in which the left atrium (cor triatriatum sinistrum) or right atrium (cor triatriatum dextrum) is divided into two compartments by a fold of tissue, a membrane, or a fibromuscular ...
Vivek Jaswal, Pratyaksha Rana, Vidur Bansal, Krishna Prasad Gourav, Arun Sharma, Shyam Kumar Singh Thingnam   +5 more
doaj   +1 more source

Cor triatriatum sinister with situs inversus totalis in an infant. [PDF]

, 2012
Cor triatriatum sinister is a rare congenital cardiac malformation characterized by a membrane in the left atrium which separates the left atrium into the proximal and distal chambers.Association of cor triatriatum is extremely rare with situs inversus
Gadekar, A., Meshram, Sushant, Pathak, Swanand, Taksande, Amar M.   +3 more
core   +1 more source

Transcatheter occlusion of a persistent left superior vena cava to the left atrium using the transseptal approach [PDF]

, 2014
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/102167/1/ccd24884 ...
Bonardi, Butera, Duff, Geva, Heye, Ootaki, Quaegebeur, Raghib, Reddy, Shah, Troost, Vizzardi, Webb   +12 more
core   +1 more source

Fetal Diagnosis of Hypoplastic Left Heart Syndrome With Restrictive Atrial Septum—Atrial Septal Morphology, Associated Lung Disease and Outcomes

Prenatal Diagnosis, Volume 46, Issue 2, Page 183-192, February 2026.
ABSTRACT Objective Fetuses with hypoplastic left heart syndrome (HLHS) and restrictive/intact atrial septum (RAS) have high mortality, partly due to pulmonary lymphangiectasia (PL). This study aimed to characterize atrial septal morphology in fetuses with HLHS and RAS and evaluate the impact of fetal intervention on PL and outcomes.
Sofie Dannesbo, Gloria Ho, Mike Seed, Vitor Guerra, Rajiv Chaturvedi, Andrew C. Cook, Niels Vejlstrup, Kasper Iversen, Henning Bundgaard, Lindsay R. Freud   +9 more
wiley   +1 more source