Arrhythmogenic Right Ventricular Cardiomyopathy and Cor Triatriatum Dexter: An Unreported Association [PDF]
Clinical Case ReportsWe 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.
Erica Franco +3 more
doaj +2 more sources
Multimodality imaging of cor triatriatum dexter complicated with hypertrophic cardiomyopathy of restrictive phenotype [PDF]
Radiology 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 +2 more sources
Percutaneous Balloon Dilation in Two Dogs with Cor Triatriatum Dexter [PDF]
Veterinary Sciences, 2022 Percutaneous balloon dilation was performed in a Rhodesian Ridgeback and in an American Staffordshire Terrier affected by cor triatriatum dexter (CTD). Both cases had ascites without jugular venous distension or pleural effusion.
Valentina Patata +7 more
doaj +2 more sources
Different Cardiac Anomalies in Mother and Son with 4q-Syndrome [PDF]
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.
Angela Guarina +3 more
core +8 more sources
Cor Triatriatum Dexter Associated with an Ostium Primum Atrial Defect and Left-Sided Opening of the Coronary Sinus in a Stillborn Fetus [PDF]
Journal of Cardiovascular Development and Disease, 2023 Cor triatriatum is a very rare cardiac malformation characterized by the presence of an abnormal interatrial membrane separating either the left or right atrial chamber into two compartments.
Silvia Farkašová Iannaccone +5 more
doaj +2 more sources
Cor Triatriatum Dexter: Contrast Echocardiography Is Key to the Diagnosis of a Rare but Treatable Cause of Neonatal Persistent Cyanosis [PDF]
Children, 2022 Cor triatriatum dexter (CTD) is an extremely uncommon and underreported congenital cardiac anomaly in which the persistence of the embryonic right venous valve separates the right atrium into two chambers with varying degrees of obstruction to antegrade ...
Irene Picciolli +13 more
doaj +2 more sources
Cor triatriatum dexter associated to Ebstein anomaly with tricuspid double lesion and atrial septal defect [PDF]
Archivos de Cardiología de México, 2021 Female 23-year-old patient with heart murmur diagnosed in the first year of life. She attended to our institute with progressive dyspnea and palpitations of 7-month evolution. Physical examination showed perioral and distal cyanosis with digital clubbing,
Ricardo Álvarez-Santana +4 more
doaj +2 more sources
A Rare Complication During Transcatheter Closure of Double Atrial Septal Defects With Incomplete Cor Triatriatum Dexter: A Case Report [PDF]
Frontiers in Cardiovascular Medicine, 2022 The cor triatiatum dexter is an embryologic remnant derived from the right atrium and totally separate from the right atrium. An incomplete cor triatiatum dexter (iCTD) means a partially obstructive remnant at the right atrium.
Ping-Hong Chen +11 more
doaj +2 more sources
COR TRIATRIATUM DEXTER EN LA EDAD ADULTA / Cor triatriatum dexter in adulthood [PDF]
CorSalud, 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
A Rare Case: Cor Triatriatum Dexter
Southern 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