Results 11 to 20 of about 200,194 (156)
Atrialised right ventricular myxoma in a patient with Ebstein’s anomaly [PDF]
Echo Research and Practice, 2018 Ebstein’s anomaly is a rare entity affecting around 1 in 200,000 live births and accounts for less than 1% of congenital heart diseases. Ebstein’s anomaly with an associated right-sided myxoma is extremely rare, with only one other case report found in ...
T-J John +3 more
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A Rare Manifestation of Asymptomatic Ebstein’s Anomaly with Tricuspid Valve Endocarditis [PDF]
Case Reports in Cardiology, 2017 Ebstein’s anomaly is a rare congenital heart disease that presents with apical displacement of the septal and posterior leaflets of the tricuspid valve. It has a wide spectrum of clinical presentations and has been shown to manifest itself any time from ...
Carmel Moazez +3 more
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Ebstein’s Anomaly, Left Ventricular Noncompaction, and Sudden Cardiac Death [PDF]
Case Reports in Cardiology, 2015 Ebstein’s anomaly is a congenital disorder characterized by apical displacement of the septal leaflet of the tricuspid valve. Ebstein’s anomaly may be seen in association with other cardiac conditions, including patent foramen ovale, atrial septal ...
Michael McGee +2 more
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Journal of Cardiovascular Magnetic Resonance, 2018 Background Myocardial fibrosis is a common pathophysiological process that is related to ventricular remodeling in congenital heart disease. However, the presence, characteristics, and clinical significance of myocardial fibrosis in Ebstein’s anomaly ...
Dan Yang +12 more
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Neonatal Ebstein’s Anomaly: Surgical Decision Making [PDF]
The Annals of African Surgery, 2018 Ebstein’s Anomaly (EA) is a rare form of congenital heart disease. Surgical decision-making in neonates is controversial. In developing countries, neonates with Ebstein’s anomaly requiring surgical intervention rarely present to health institutions ...
Awori M, Mutwiri RK, Mutunga WM, Jowi SO
doaj +2 more sources
Image to Fit the Clinical Picture: Point-of-care Ultrasound Assessment of Ebstein’s Anomaly in Peru [PDF]
Clinical Practice and Cases in Emergency Medicine, 2020 Ebstein’s anomaly is a congenital heart defect that when left untreated can lead to unique physical exam and ultrasound findings. This case describes a patient who presented with dyspnea and was found to have cyanosis, clubbing, and dilation of right ...
Ashley C. Rider +2 more
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Case Reports in Pediatrics, 2021 Ebstein’s anomaly is characterized by the apical displacement of the septal and posterior leaflets of the tricuspid valve with atrialization of the right ventricle (RV).
Mohammad Mehdi +3 more
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Historical and modern aspects of surgical treatment of Ebstein’s anomaly [PDF]
Бюллетень сибирской медицины, 2020 Congenital heart defects (CHDs) are recognized as the most common type of congenital pathology. The frequency of CHDs reaches 2.4–14.2 % per 1 000 newborns.
N. M. Troshkinev +5 more
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Antenatal Diagnosis of a Partial Atrioventricular Canal with Ebstein’s Anomaly
Children, 2021 The simultaneous occurrence of an atrioventricular canal defect (AVCD) and Ebstein’s anomaly is extremely rare, occurring in less than 0.5% of all patients with AVCD. Only 22 cases are described in the literature.
Gerald Laforest +4 more
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Postoperative persistent diastolic dyssynchronous expansion in patients with Ebstein's anomaly.
PLoS ONE, 2019 In Ebstein's anomaly, maximal expansion in the atrialized right ventricle (RV) occurs during early diastole, whereas that of the functional RV occurs in late diastole, resulting in diastolic dyssynchronous expansion (DSE).
Kyung-Jin Kim +3 more
doaj +2 more sources