Results 61 to 70 of about 160,338 (112)
Different Cardiac Anomalies in Mother and Son with 4q‐Syndrome
Case Reports in Genetics, Volume 2015, Issue 1, 2015., 2015 We report a female patient with asymptomatic cor triatriatum sinister, associated with 4q34.3 deletion. Her child, carrying the same imbalance, suffers from tetralogy of Fallot. To the best of our knowledge, this is the first reported case of cor triatriatum associated with deletion of the long arm of the chromosome 4; furthermore, the majority of ...
Marcello Marcì +4 more
wiley +1 more source
CHRISMED Journal of Health and Research, 2019 Infants of diabetic mothers are prone to cardiac malformations due to teratogenicity of diabetes mellitus (DM). We present here the case of a macrosomic neonate who had marked difficulty with breathing.
Igoche David Peter +5 more
doaj +1 more source
Pulmonary‐Esophageal Variceal Bleeding: A Unique Presentation of Partial Cor Triatriatum Sinistrum
Case Reports in Vascular Medicine, Volume 2013, Issue 1, 2013., 2013 Cor triatriatum sinistrum is a rare congenital disorder defined as a division of the left atrium by a diaphragmatic membrane resulting in two left atrial chambers. The membranous division of the atrium can be partial or complete and can affect either atrium, with involvement of the right atrium referred to as cor triatriatum dexter.
Fortune O. Alabi +6 more
wiley +1 more source
Cor triatriatum dexter and tricuspid valve stenosis in an 8 month old Labrador Retriever
, 2008 Case Description: Cor Triatriatum Dexter and Tricuspid Valve Stenosis in an 8 month old Labrador retriever with signs of right sided congestive heart failure.
Lim, Frolich N.
core +6 more sources
Cor Triatriatum Sinister in a French Bulldog
Case Reports in Veterinary Medicine, Volume 2012, Issue 1, 2012., 2012 A 3‐year‐old male French Bulldog was evaluated due to recent history of intolerance to exercise and coughing. The clinical, radiographic, and echocardiographic findings were consistent with cor triatriatum sinister (CTS), a congenital heart anomaly in which the left atrium is subdivided into two compartments by an abnormal fibromuscular membrane.
Gustavo L. G. Almeida +7 more
wiley +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
Taksande, Amar M. +3 more
core
[Cor triatriatum dexter of an adult].
, 1998 Cor triatriatum dexter is a rare congenital malformation in which a membrane divides the right atrium into two chambers. The membrane represents a persistence of the right sinus venosus valve (RSV).
Rickli H, Wyss E, Jenni R, Ammann P
core +1 more source
Cor triatriatum dexter of unusual morphology in a miniature schnauzer [PDF]
, 2022 A five-year-nine-month-old, male entire, miniature schnauzer presented for further investigation of pleural effusion. Echocardiography revealed a perforated membrane dividing the right atrium into two chambers: the true right atrium (a small, lower ...
Neves, J +4 more
core +1 more source
An isolated fetal cor triatriatum dexter during a targeted anatomic survey at 22 weeks’ gestation [PDF]
, 2008 Cor triatriatum dexter is a rare cardiac malformation characterized by division of the right atrium into two compartments by a usually fenestrated membrane, whose degree of partitioning or septation is responsible for different clinical manifestations ...
Cignini, Pietro +3 more
core +1 more source
Journal of Veterinary Internal Medicine, Volume 39, Issue 5, September/October 2025.ABSTRACT Background Determining right ventricular (RV) volume typically requires three‐dimensional imaging due to its complex shape. The ellipsoid model offers a two‐dimensional alternative, employing area‐ or linear‐based formulas with further variations depending on the echocardiographic views used for measurements.
Robert Ciardullo +5 more
wiley +1 more source