Results 21 to 30 of about 1,273 (168)

Cor Triatriatum Dexter: An Innocent Bystander

Methodist DeBakey Cardiovascular Journal, 2022
Cor triatriatum dexter is a rare congenital heart defect with a varied clinical presentation ranging from asymptomatic to right heart failure. Accurate diagnosis is imperative as it may affect clinical decision making.
Stephanie C. Fuentes Rojas, Gerald Lawrie, Nadeen N. Faza   +2 more
doaj   +1 more source

Insights into the perinatal phenotype of Kabuki syndrome in infants identified by genome‐wide sequencing

American Journal of Medical Genetics Part A, Volume 191, Issue 4, Page 930-940, April 2023., 2023
Abstract Increasing use of unbiased genomic sequencing in critically ill infants can expand understanding of rare diseases such as Kabuki syndrome (KS). Infants diagnosed with KS through genome‐wide sequencing performed during the initial hospitalization underwent retrospective review of medical records.
Kristen Wigby, Monia Hammer, Mari Tokita, Priyanka Patel, Marilyn C. Jones, Austin Larson, Frances Velez Bartolomei, Natalie Dykzeul, Anne Slavotinek, Tiffany Yip, Sara Bandres‐Ciga, Brittany N. Simpson, Kristen Suhrie, Suma Shankar, Regan Veith, Jennifer Bragg, Cynthia Powell, Stephen F. Kingsmore, David Dimmock, Jill Maron, Jonathan Davis, Miguel Del Campo   +21 more
wiley   +1 more source

Atrial Fibrillation Ablation in a Patient with Cor Triatriatum Sinister and Left Common Pulmonary Vein: Impact of Left Atrium Anatomy on Ablation Approach

Life, 2022
Atrial fibrillation is the most common presentation in adult patients with cor triatriatum sinister. The key to successful and safe catheter ablation in these patients is an accurate exploration and thorough understanding of the left atrial anatomy, both
Ioan-Alexandru Minciună, Gabriel Cismaru, Mihai Puiu, Radu Roșu, Denis Amet, Daniela Anghelina, Alexandra Gica, Raluca Tomoaia, Marius Andronache, Dana Pop   +9 more
doaj   +1 more source

Cor triatriatum and stroke [PDF]

BMJ Case Reports, 2017
Cor triatriatum sinistrum (CTS) is a congenital anomaly where the left atrium is divided into two compartments by a fibromuscular membrane. This report aims to add to the literature on a rare cardiac condition that can cause neurological morbidity.
Jose Danilo Bengzon Diestro, Joseph Justin Hipolito Regaldo, Eddieson Masangcay Gonzales, Maria Kristina Casanova Dorotan, Adrian Isidoro Espiritu, Jose Leonard Rivera Pascual   +5 more
openaire   +2 more sources

Cor triatriatum sinister: a case series

Türk Kardiyoloji Derneği Arşivi, 2016
Objective: As a highly rare congenital defect, cor triatriatum sinister represents only 0.1% of congenital cardiac anomalies. Depending on the degree of obstruction and the accompanying symptoms, cor triatriatum can be diagnosed at any age.
Onur Isik, Muhammet Akyuz, Mehmet Fatih Ayik, Erturk Levent, Yuksel Atay   +4 more
doaj   +1 more source

Cor triatriatum simulating a left atrial mass in adult patient

Radiology Case Reports, 2023
We report a case of non-thrombosed cor triatriatum sinister simulating a cardiac mass on thoracic CT angiogram in a 58-year-old man presenting with acute chest pain.
Alexandre Semionov, MD, PhD, Juan Batlle, MD, Karl Sayegh, MD   +2 more
doaj   +1 more source

A rare cause of cyanosis in neonatal age: Cor triatriatum dexter

Annals of Pediatric Cardiology, 2022
Cor triatriatum dexter is an extremely rare congenital anomaly that is caused by the partitioning of the right atrium by a broad sheet of tissue due to the persistence of the right sinus venosus valve.
Adriano Caputo, Mario Giordano, Carola Iacono, Guido Oppido, Maria Giovanna Russo   +4 more
doaj   +1 more source

Subtotal cor triatriatum sinister associated with bilateral partial anomalous pulmonary venous return

Türk Kardiyoloji Derneği Arşivi, 2016
Cor triatriatum sinister is a rare congenital cardiac pathology, representing only 0.1% of congenital cardiac anomalies, and often associated with other cardiac defects.
Onur Işık, Muhammet Akyuz, Mehmet Fatih Ayık, Yuksel Atay   +3 more
doaj   +1 more source

Clinical case of Cor triatriatum sinister, a dilemma of anticoagulation: A case report and literature review. [PDF]

Clin Case Rep
Key Clinical Message Cor triatriatum is a rare congenital heart abnormality in which a membrane separates the left atrium (LA; sinister) or the right atrium (dexter) into two compartments. It is also a long‐forgotten cause of atrial fibrillation (AF) and substantially higher rates of blood stagnation, particularly proximal to the additional septum in ...
Arzhangzade A, Zamirian M, Nozhat S, Shafei S, Narimani Javid R, Salahi S, Khorshidi S.   +6 more
europepmc   +2 more sources

Wong's anomaly – A rare variant of cor triatriatum

Indian Heart Journal, 2015
Cor triatriatum sinistrum is an extremely rare congenital heart disease. It is even more uncommon in adults, and clinically significant mitral valve lesion complicating cor triatriatum is distinctly rare.
K. Jayaprakash, Suresh Madhavan, V. Sudha Kumary, Raju George, Nigil Cletus, S. Baiju   +5 more
doaj   +1 more source