Results 61 to 70 of about 239,154 (181)

Transcatheter pulmonary valve implantation in tetralogy of Fallot and Ebstein's anomaly with one and a half ventricular repair

, 2021
The coexistence of tetralogy of Fallot and Ebstein's anomaly is extremely rare. There are only a few case reports in the literature, and surgical options for the treatment are controversial.
Ugan Atik, Sezen, Guzeltas, Alper, Tanidir, Ibrahim Cansaran, Sezen Ugan Atik, Alper Guzeltas, Ibrahim Cansaran Tanidir   +5 more
core   +1 more source

Defining Features of Gabriele‐de Vries Syndrome in Adults: A Case Report and Literature Review

American Journal of Medical Genetics Part A, Volume 200, Issue 10, Page 2396-2404, October 2026.
ABSTRACT Gabriele‐de Vries syndrome (GADEVS) is a neurodevelopmental disorder caused by heterozygous pathogenic variants in the YY1 gene. Like most rare genetic syndromes, the adult manifestations of GADEVS remain poorly defined. Here, we describe the oldest patient reported to date with GADEVS—a 63‐year‐old woman with a c.1177_1179del YY1 variant ...
Ethan W. Hollingsworth, Changrui Xiao
wiley   +1 more source

Antenatal Imaging of Ebstein’s Anomaly with Hydrops Fetalis

Medical Journal of Dr. D.Y. Patil Vidyapeeth
Ebstein’s anomaly is a rare congenital cardiac anomaly characterized by tricuspid valve (TV) malformation, including the low insertion of the septal and posterior leaflets of the TV into the tricuspid annulus. It is one of the common malformations of the
Shrishail Adke, Harshitha H. Shetty, Hemangini Thakkar   +2 more
doaj   +1 more source

Coexistence of Ebstein Anomaly and Cerebral Cavernous Malformation: A Case Report

Clinical Case Reports, Volume 14, Issue 10, October 2026.
ABSTRACT In most patients who have Ebstein anomaly (EA), neurological symptoms are either associated with thromboembolic episodes or due to arrhythmic complications. Cerebral cavernous malformation (CCM) is a vascular anomaly made up of sinusoidally dilated blood vessels, often presenting with seizure activity or intracranial bleeding.
Nazmin Ahmed, Mohaiminul Islam, Md. Raad Kazi, Jubair Ahmed Sikder, Tajrian Sultana, Mohammad Nazrul Hossain   +5 more
wiley   +1 more source

Catheter ablation of arrhythmias in Ebstein's anomaly: a multicenter study

, 2011
In patients with Ebstein's anomaly (EA) arrhythmias are frequently encountered. Although most arrhythmias can be targeted with catheter ablation, specific issues render the procedure more challenging in EA.
Szili-Torok, T (Tamás), Zimmermann, Marc, NATASJA DE GROOT, Delacretaz, E, Jensen, HK, Szili-Torok, Tamas, Nielsen, Jens Cosedis, PETER LUKAC, LAURENT ROTEN, Lukac, Peter, HENRIK KJAERULF JENSEN, Zimmermann, M, Roten, L, Nielsen, JC, JENS COSEDIS NIELSEN, Roten, Laurent, Lukac, P, ETIENNE DELACRÉTAZ, TAMAS SZILI-TOROK, DE Groot, Natasja, Delacrétaz, Etienne, MARC ZIMMERMANN, Jensen, Henrik Kjaerulf, Zimmermann M, Delacrétaz E, Nielsen JC, Lukac P, Jensen HK, DE Groot N, Roten L, Szili-Torok T   +30 more
core   +1 more source

Anomalia de Ebstein da válvula tricúspide. Tolerância clínca até aos 38 anos de idade e ao estado de gravidez.

Acta Médica Portuguesa, 1994
Ebstein's Anomaly of the tricuspid valve has a variable degree of abnormality with a continuous change between mild and severe forms and, consequently, a variable clinical course. Pregnancy can also be well tolerated with a good fetal outcome.
J M Santos, M Esteves, M J Silva, E Silva, M A Barbosa, A G da Palma-Carlos   +5 more
doaj   +1 more source

Standardized Reporting of Cardiac Magnetic Resonance Examinations in Children With Cardiac Diseases and Adults With Congenital Heart Disease: A Scientific Statement From the Association for European Pediatric and Congenital Cardiology (AEPC) and the International Society for Magnetic Resonance in Medicine (ISMRM)

Journal of Magnetic Resonance Imaging, EarlyView.
Francesca Raimondi, Inga Voges, Lamia Ait‐Ali, Sonya Babu‐Narayan, Rene Botnar, Barbara Burkhardt, Adrienne Campbell‐Washburn, Dominik Daniel Gabbert, Georg Hansmann, Willem A. Helbing, Hasan Hosan, Sylvia Krupickova, Heiner Latus, Duarte Martins, Colin McMahon, Christian Meierhofer, Vivek Muthurangu, Tiina Ojala, Pim van Ooij, Claudia Prieto, Milan Prsa, Kuberan Pushparajah, José F. Rodríguez Palomares, Samir Sarikouch, Lars Grosse‐Wortman, F. Gerald Greil, Heynric Grotenhuis   +26 more
wiley   +1 more source

The impacts of energy and protein provision on anthropometric changes in infants with critical congenital heart disease

Journal of Pediatric Gastroenterology and Nutrition, Volume 83, Issue 4, Page 737-743, October 2026.
Abstract Objectives Malnutrition in patients with critical congenital heart disease (CCHD) is associated with worse outcomes, however, feeding challenges, and changes in metabolic demands obscure the relationship between nutrient intake and growth in this patient population.
Colin R. Tang‐Whitmore, Cydney Coleman, Brittany Faanes, Laura Gearman, Brian F. Joy, Stacie Knutson, Benjamin W. Langworthy, Katie M. Pfister, Catherine Larson‐Nath   +8 more
wiley   +1 more source

Electrocardiographic characteristics of patients with Ebstein's anomaly before and after ablation of an accessory atrioventricular pathway

, 2006
UNLABELLED The abnormal development of the tricuspid valve in patients with Ebstein's anomaly results in several activation abnormalities including delayed intraatrial conduction, right bundle branch block (RBBB), and ventricular preexcitation.
Victoria, Diana, LUIS COLIN, Gonzalez, Mario D., Iturralde, Pedro, Márquez, Manlio F., Nava, Santiago, Sálica, Gabriel, PEDRO ITURRALDE, SANTIAGO NAVA, ALFREDO DE MICHELI, De Micheli, Alfredo, Medeiros Domingo, Argelia, MANLIO F. MÁRQUEZ, DIANA VICTORIA, MARIO D. GONZALEZ, Colin, Luis, ARGELIA MEDEIROS, GABRIEL SÁLICA   +17 more
core   +1 more source

Long‐Term Follow Up of Two Patients With Variants in the Cluster 1031‐1159 of TRRAP Gene: Expanding the Phenotype of Developmental Delay With or Without Dysmorphic Facies and Autism

American Journal of Medical Genetics Part A, Volume 200, Issue 9, Page 2099-2105, September 2026.
ABSTRACT The transformation/transcription domain‐associated protein (TRRAP) gene encodes a large multidomain protein, a member of the phosphatidylinositol 3‐kinase‐related kinase (PIKK) family. TRRAP is a component of the histone acetyltransferase (HAT) complex, and it plays an important role in gene transcription, DNA repair, and cell‐cycle regulation.
Roseli Maria Zechi‐Ceide, Vinicius Contrucci Dantas Segarra, Siulan Vendramini‐Pittoli, Henrique Regonaschi Serigatto, Luiza Virmond, Heloisa Marcelina da Cunha Palhares, Fernanda Jehee, Ana Cristina Victorino Krepischi, Carla Rosenberg, Carlos Henrique Paiva Grangeiro, Nancy Mizue Kokitsu‐Nakata   +10 more
wiley   +1 more source