Results 31 to 40 of about 822 (143)

246. Transposición de grandes arterias – simple tardía: corrección anatómica con regresión del ventrículo izquierdo

Cirugía Cardiovascular, 2012
CiJustificación: en los lactantes mayores de 2 meses con una transposición de grandes arterias (TGA) simple, el switch arterial se asocia a un riesgo elevado de mortalidad por disfunción del ventrículo izquierdo. Material y métodos: presentamos dos casos
M.T. Conejero Jurado, C. Merino Cejas, J. Casares Mediavilla, J. Otero Forero, D. Valencia Núñez, P. Maiorano Iuliano, G. Sauchelli Faas, I. Pernia Oreña, P. Alados Arboledas, J. Moya González, M. Román Ortiz   +10 more
doaj   +1 more source

Truncus Arteriosus - modified Van Praagh’s Type 3A and Anesthesia: a case report.

Ain Shams Journal of Anesthesiology, 2020
Background One of the rare complex congenital anomalies is truncus arteriosus—modified Van Praagh’s type 3A. Survival of this type of truncus arteriosus child beyond infancy without surgical treatment is unreported.
Vinodhadevi Vijayakumar, Sampathkumar Muthuramalingam, Arimanickam Ganesamoorthi   +2 more
doaj   +1 more source

Coexisting ADAR and TSHB Mutations in an Infant With Retinal Detachment and Transient Cardiomyopathy

Case Reports in Endocrinology, Volume 2026, Issue 1, 2026.
Background Central congenital hypothyroidism (C‐CH) due to thyroid‐stimulating hormone beta (TSHB) variants is rare and often missed by thyroid‐stimulating hormone (TSH)–based neonatal screening. Adenosine deaminase acting on RNA (ADAR)‐related Aicardi–Goutières syndrome type 6 (AGS6) is an interferonopathy with early‐onset encephalopathy.
Tamer Draidi, Mohammad Khalil, Abed Kabaha, Rafat Zuriqi, Mohammad Masu’d, Osamu Isozaki   +5 more
wiley   +1 more source

Dupla via de saída do ventrículo direito com comunicação interventricular não relacionada: resultados da correção cirúrgica com técnica de múltiplos retalhos

Brazilian Journal of Cardiovascular Surgery, 1997
Objetivo: Apresentar uma modificação técnica para a correção cirúrgica biventricular da dupla via de saída de ventrículo direito com comunicação interventricular não relacionada.
Miguel BARBERO-MARCIAL, Carla TAMANATI, Marcelo B. JATENE, Vera D. AIELLO, José Augusto BAUCIA, Edmar ATIK, Luiz J. KAJITA, Munir EBAID, Geraldo VERGINELLI, Adib D. JATENE   +9 more
doaj   +1 more source

The Trace of c.3747_3748insGG Variation of the MYBPC3 Gene in the Family With Atrioventricular Canal Defect

Cardiology Research and Practice, Volume 2026, Issue 1, 2026.
Background Atrioventricular canal defect (AVCD) is a congenital heart disease often associated with genetic changes, with a broad spectrum of anatomical patterns. Aim We present a novel likely pathogenic variant of MYBPC3 in a proband with AVCD. Methods A clinical and genetic evaluation was conducted on a one‐year‐old Iranian girl referred to our ...
MohammadHossein MozafaryBazargany, Maryam Pourirahim, Alireza Salmanipour, Kasra Mehdizadeh, Mohammad Mahdavi, Mohammadrafie Khorgami, Majid Maleki, Samira Kalayinia, Irfan Ahmad   +8 more
wiley   +1 more source

Situs inversus with levocardia and congenitally corrected transposition of great vessels with rheumatic tricuspid valve stenosis and regurgitation

Heart Views, 2011
Congenitally corrected transposition of great arteries is a rare congenital anomaly. This case report describes a 30-year-old patient of congenitally corrected transposition of the great arteries with rheumatic involvement of systemic (tricuspid) atrio ...
Bharat B Kukreti, S Ramakrishnan, Balram Bhargava   +2 more
doaj   +1 more source

Prenatal diagnosis and array comparative genomic hybridization characterization of trisomy 21 in a fetus associated with right congenital diaphragmatic hernia and a review of the literature of chromosomal abnormalities associated with congenital diaphragmatic hernia

Taiwanese Journal of Obstetrics & Gynecology, 2015
Objective: Rapid genome-wide aneuploidy diagnosis using uncultured amniocytes and array comparative genomic hybridization (aCGH) is useful in pregnancy with abnormal ultrasound findings.
Chih-Ping Chen, Yeou-Lih Wang, Schu-Rern Chern, Yu-Peng Liu, Cheng-Ran Peng, Yu-Ling Kuo, Peih-Shan Wu, Wen-Lin Chen, Wayseen Wang   +8 more
doaj   +1 more source

Robot-assisted distal gastrectomy with lymph node dissection for gastric cancer in a patient with situs inversus partialis: a case report with video file

Surgical Case Reports, 2018
Background Situs inversus is a rare congenital condition that is currently classified into two types: complete situs inversus (situs inversus totalis, SIT) and partial situs inversus (situs inversus partialis, SIP).
Yuki Aisu, Yoshio Kadokawa, Shigeru Kato, Daiki Yasukawa, Yusuke Kimura, Tomohide Hori   +5 more
doaj   +1 more source

Assessment of Double Outlet Left Ventricle in Pediatrics Using Transthoracic Echocardiography and Computed Tomographic Angiography

Pediatric Discovery, Volume 3, Issue 4, December 2025.
The clinical manifestation of DOLV was atypical. TTE has a relatively high diagnostic accuracy for DOLV in pediatric, which is very valuable for its early detection. ABSTRACT Double outlet left ventricle (DOLV) is a rare congenital cardiac anomaly in which both great arteries originate entirely or predominantly from the morphologic left ventricle.
Xu Zhu, Guangyi Zhong, Xiaojuan Ji, Xue Xiang, Min Zheng, Huina Yan, Rui Li   +6 more
wiley   +1 more source

CRISS - CROSS HEART (Report of four cases)

Majalah Kardiologi Indonesia, 2013
Criss-cross heart is a rare congenital cardiac anomaly characterized by crossing of the inflow streams of the two ventricles. The anomaly seems to be due to abnormal twisting of the heart about its long axis and when the axis of the openings of the ...
Anna Ulfah Rahajoe, Poppy S Roebiono, Muhammad B Fahmi, Ganesja M Harimurti   +3 more
doaj   +1 more source