Results 91 to 100 of about 2,596 (202)

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

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

2021 ACVIM Forum Research Abstract Program

, 2021
Journal of Veterinary Internal Medicine, Volume 35, Issue 6, Page 2943-3079, November/December 2021.
wiley   +1 more source

Intraoperative 2D and 3D transesophageal echocardiographic assessment of cor triatriatum with ostium secundum atrial septal defect in an adult patient

Annals of Cardiac Anaesthesia, 2020
Cor triatriatum is a rare congenital cardiac anomaly. Majority of the cases present in the childhood with an incidence of 0.4%. However, we report a case of cor triatrium sinister with ostium secundum atrial septal defect (ASD) in a 39-year-old female ...
Rahul Shabadi, Pushkar Desai, Suresh Chengode   +2 more
doaj   +1 more source

Arrhythmogenic Right Ventricular Cardiomyopathy and Cor Triatriatum Dexter: An Unreported Association

Clinical Case Reports, Volume 13, Issue 10, October 2025.
ABSTRACT We present a 74‐year‐old patient with a previous diagnosis of arrhythmogenic right ventricular cardiomyopathy manifesting as heart failure where a concomitant cor triatriatum dexter has accidentally been diagnosed by echocardiography. The association between arrhythmogenic right ventricular cardiomyopathy and cor triatriatum dexter has not ...
Erica Franco, Chiara Rovera, Claudio Moretti, Pier Paolo Bassareo   +3 more
wiley   +1 more source

Dotychczas bezobjawowe dwumiesięczne niemowlę z unikatową prezentacją trójprzedsionkowego lewego serca, prawego częściowego nieprawidłowego spływu żył płucnych oraz krytycznej nadzastawkowej stenozy mitralnej [PDF]

, 2019
Major developments in diagnostic techniques in pre- and neonatal care have significantly reduced the rate of undetected congenital heart defects (CHD). Despite such advances, several patients with critical congenital heart defects are discharged annually
Moll, Jacek, Moll, Jadwiga A., Ostrowska, Katarzyna, Pawliczak, Filip   +3 more
core   +2 more sources

Echocardiographic Changes Related to Pulmonary Hypertension in Preweaned Dairy Calves With Bronchopneumonia: A Case–Control Study in Commercial Dairy Farms

Journal of Veterinary Internal Medicine, Volume 39, Issue 2, March/April 2025.
ABSTRACT Background Bronchopneumonia (BP) can cause pulmonary hypertension (PH) and secondary cardiovascular changes. Objectives The aim of this study was to describe PH–related transthoracic Doppler echocardiography (TTE) changes in preweaned dairy calves with BP diagnosed by thoracic ultrasonography (TUS).
Sara Ghilardi, Giulia Sala, Chiara Locatelli, Davide Pravettoni, Mara Bagardi, Antonio Boccardo   +5 more
wiley   +1 more source

Robotic Congenital Cardiac Surgery Practice Worldwide: A Systematic Review

Journal of Cardiac Surgery, Volume 2025, Issue 1, 2025.
Background: With the increasing adoption of robotic technology in adult cardiac surgery patients, improved surgeon experience and wider utilization have been reported. However, interpreting trends in robotic congenital surgery is more challenging.
Madonna E. Lee, Andrea Amabile, Irbaz Hameed, James Antonios, Ahmed K. Awad, Alexandria Brackett, Markus Krane, Peter J. Gruber, Arnar Geirsson, Tomás A. Salerno   +9 more
wiley   +1 more source

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

Radiology 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, Murad Azamtta, MD, Qutaiba Ja'far A. Mahmoud, MD   +2 more
doaj   +1 more source

Atrial Fibrillation and Cor Triatriatum Sinister: A Case Report [PDF]

The Permanente Journal, 2015
A 29-year-old man presented to our hospital with palpitations, shortness of breath, and orthopnea. After being admitted, he progressed to cardiogenic shock and respiratory failure, which required ventilator support and cardioversion. Subsequent evaluation revealed a fibromuscular membrane across the left atrium, requiring urgent corrective surgery.
Hoa Jeannie, Tran, Robert, Gordon, Thomas, Alloggiamento, Sukhvinder Kaur, Nagi, Ashok, Krishnaswami   +4 more
openaire   +2 more sources