Results 101 to 110 of about 221,247 (223)

Treatment of non-restrictive cor triatriatum sinister during concomitant cardiac surgery

The Cardiothoracic Surgeon, 2022
Background Cor triatriatum is a rare congenital heart disease representing the 0.4% of all congenital cardiac anomalies. To date, no specific genetic alteration has been associated to cor triatriatum. The left-sided presentation (cor triatriatum sinister
Lorenzo Di Bacco, Michele D’Alonzo, Alberto Repossini, Francesca Zanin, Claudio Muneretto, Stefano Benussi   +5 more
doaj   +1 more source

Impact of isolated fetal congenital heart disease on pregnancy and perinatal outcomes

International Journal of Gynecology &Obstetrics, Volume 168, Issue 2, Page 790-799, February 2025.
Abstract Objective The aim of the present study was to evaluate the obstetric complications associated with isolated fetal congenital heart disease (CHD) by comparing pregnancies with and without this condition. Methods In this retrospective matched comparative study at Siriraj Hospital, Thailand, we included 233 postnatally confirmed fetal CHD cases ...
Yossawadee Kittiratanapinan, Sanitra Anuwutnavin, Supaluck Kanjanauthai, Punnanee Wutthigate, Dittakarn Boriboonhirunsarn, Saifon Chawanpaiboon   +5 more
wiley   +1 more source

Staged Norwood operation for patients with hypoplastic left heart syndrome and cor triatriatum: a report of two cases

General Thoracic and Cardiovascular Surgery Cases
Two patients with hypoplastic left heart syndrome (HLHS) concomitant with cor triatriatum underwent the staged Norwood procedure following hybrid palliation. Cor triatriatum was diagnosed after birth in both cases.
Yukino Iijima, T. Hoashi, T. Kojima, H. Nagase, Yuji Fuchigami, Takaaki Suzuki   +5 more
semanticscholar   +1 more source

Cor triatriatum sinister e hipertensão arterial pulmonar secundária em cão

Arquivo Brasileiro de Medicina Veterinária e Zootecnia, 2014
This paper describes the occurrence of cor triatriatum sinister, a rare cardiac malformation in dogs, associated with pulmonary edema and pulmonary hypertension in a 5-year-old Poodle female with history of acute dyspnea and cyanosis.
T. Champion, F.N. Gava, E. Garrido, A.L.B. Galvão, A.A. Camacho   +4 more
doaj   +1 more source

Anesthetic management of non-cardiac surgery with adult onset type of cor triatriatum sinister -A case report- [PDF]

Korean Journal of Anesthesiology, 2011
A 45-year-old woman with cor triatriatum sinister was admitted for laparoscopic resection of an ovarian tumor. Her medical history was benign with the exception of a single episode of syncope one year ago.
Hae Mi Lee, Hyun Suk Sung, Sae Yeon Kim
doaj   +1 more source

The Prevalence and Clinical Characteristics of PHACE Syndrome in Facial Segmental Hemangiomas: A Single‐Center Retrospective Study

Dermatologic Therapy, Volume 2025, Issue 1, 2025.
Introduction PHACE syndrome is a neurocutaneous syndrome characterized by large facial segmental hemangiomas as the most typical manifestation. Its prevalence in East Asian is not well studied. Methods The retrospective study included 98 infants with facial segmental hemangiomas who underwent brain MRI/MRA, cardiac ultrasound, and ophthalmology ...
Jingjing Sun, Rui Chang, Shih-Jen Chang, Lei Chang, Qianyi Chen, Gang Ma, Yajing Qiu, Xiaoxi Lin, Yun-Sheng Liang   +8 more
wiley   +1 more source

Serendipitous diagnosis of cor triatriatum sinister in a child with Kawasaki disease [PDF]

, 2015
Cor triatriatum is a rare congenital anomaly which has wide-ranging severity depending on the structure of the additional intra-atrial septum. We report the case of a boy who was incidentally diagnosed with cor triatriatum by echocardiography during ...
Eun, Lucy Youngmin, Choi, Jae Young, Jung, Jo Won, Jhon, Jin   +3 more
core   +1 more source

Cor triatriatum dexter: A rare cause of cyanosis during neonatal period

Annals of Pediatric Cardiology, 2016
Cor-triatriatum dexter is an extremely rare congenital heart defect in which there is complete persistence of the right valve of embryonic sinus venosus that results in partitioning of the right atrium into a smooth and trabeculated portion.
Mohammed Hussien Alghamdi
doaj   +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

Multiorgan manifestations of COL4A1 and COL4A2 variants and proposal for a clinical management protocol

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, Volume 196, Issue 4, December 2024.
Abstract COL4A1/2 variants are associated with highly variable multiorgan manifestations. Depicting the whole clinical spectrum of COL4A1/2‐related manifestations is challenging, and there is no consensus on management and preventative strategies. Based on a systematic review of current evidence on COL4A1/2‐related disease, we developed a clinical ...
Simone Gasparini, Simona Balestrini, Luigi Francesco Saccaro, Giacomo Bacci, Giorgia Panichella, Martino Montomoli, Gaetano Cantalupo, Stefania Bigoni, Giorgia Mancano, Simona Pellacani, Vincenzo Leuzzi, Nila Volpi, Francesco Mari, Federico Melani, Mara Cavallin, Tiziana Pisano, Giulio Porcedda, Augusto Vaglio, Davide Mei, Carmen Barba, Elena Parrini, Renzo Guerrini   +21 more
wiley   +1 more source