Results 151 to 160 of about 3,319 (201)
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American Heart Journal, 1997
The purpose of this study was to determine the most discriminating clinical and echocardiographic features that are most helpful in correctly identifying Ebstein's anomaly of the tricuspid valve from other causes of tricuspid regurgitation. Ebstein's anomaly is an uncommon malformation of the tricuspid valve with diagnostic echocardiographic features ...
N M, Ammash +4 more
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The purpose of this study was to determine the most discriminating clinical and echocardiographic features that are most helpful in correctly identifying Ebstein's anomaly of the tricuspid valve from other causes of tricuspid regurgitation. Ebstein's anomaly is an uncommon malformation of the tricuspid valve with diagnostic echocardiographic features ...
N M, Ammash +4 more
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The Annals of Thoracic Surgery, 1971
Abstract The surgical treatment of Ebstein's anomaly is discussed from our experience with 5 patients who underwent successful operation together with 32 previously reported patients. Tricuspid valve replacement with a disc valve and primary closure of the atrial septal defect was performed in our 5 patients.
S, Kitamura +5 more
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Abstract The surgical treatment of Ebstein's anomaly is discussed from our experience with 5 patients who underwent successful operation together with 32 previously reported patients. Tricuspid valve replacement with a disc valve and primary closure of the atrial septal defect was performed in our 5 patients.
S, Kitamura +5 more
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Annals of Internal Medicine, 1960
Excerpt A congenital anomaly consisting of downward displacement of the tricuspid valve in the right ventricle in a young man was described by Ebstein in 1866.1Several articles with collections of ...
F A, OLDENBURG, A D, NICHOL
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Excerpt A congenital anomaly consisting of downward displacement of the tricuspid valve in the right ventricle in a young man was described by Ebstein in 1866.1Several articles with collections of ...
F A, OLDENBURG, A D, NICHOL
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Seminars in Thoracic and Cardiovascular Surgery, 2017
Ebstein’s anomaly is a rare congenital heart defect that results from varying degrees of failure of delamination of the tricuspid valve leaflets from the endocardium of the right ventricle. This results in apical displacement, particularly of the septal and posterior leaflets of the tricuspid valve. The anterior leaflet is typically broad and sail-like
T K Susheel, Kumar +2 more
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Ebstein’s anomaly is a rare congenital heart defect that results from varying degrees of failure of delamination of the tricuspid valve leaflets from the endocardium of the right ventricle. This results in apical displacement, particularly of the septal and posterior leaflets of the tricuspid valve. The anterior leaflet is typically broad and sail-like
T K Susheel, Kumar +2 more
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Dealing with Ebstein's anomaly
Cardiology in the Young, 2013AbstractEbstein's anomaly is a complex congenital disorder of the tricuspid valve. Presentation in neonatal life and (early) childhood is common. Disease severity and clinical features vary widely and require a patient-tailored treatment. In this review, we describe the natural history of children and adolescents with Ebstein's anomaly, including ...
Geerdink, L.M., Kapusta, L., Kapusta, L.
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The spectrum of Ebstein's anomaly
American Heart Journal, 1967Abstract Seventeen cases of Ebstein's anomaly have been presented; the diagnosis was confirmed by autopsy in 6, and made on clinical grounds in the other 11. The series includes the youngest patient dying of the lesion, a stillborn infant, and the fifth oldest patient thus far reported (64 years).
E, Genton, S G, Blount
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Cardiology, 2008
2 adult siblings with Ebstein’s anomaly are presented in this report. The second sibling was found to have the anomaly 20 years after the first sibling was diagnosed. The use of echocardiography in screening for Ebstein’s anomaly and the diagnostic features are emphasized. Documentation by electrode catheter recording intracardiac electrocardiogram and
K S, Lo, J P, Loventhal, J A, Walton
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2 adult siblings with Ebstein’s anomaly are presented in this report. The second sibling was found to have the anomaly 20 years after the first sibling was diagnosed. The use of echocardiography in screening for Ebstein’s anomaly and the diagnostic features are emphasized. Documentation by electrode catheter recording intracardiac electrocardiogram and
K S, Lo, J P, Loventhal, J A, Walton
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Neonatal Network, 2014
Cardiac congenital abnormalities are a leading cause in neonatal mortality occurring in up to 1 in 200 of live births. Ebstein anomaly, also known as Kassamali anomaly, accounts for 1 percent of all congenital cardiac anomalies. This congenital abnormality involves malformation of the tricuspid valve and of the right ventricle.
Joseph, Galea +4 more
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Cardiac congenital abnormalities are a leading cause in neonatal mortality occurring in up to 1 in 200 of live births. Ebstein anomaly, also known as Kassamali anomaly, accounts for 1 percent of all congenital cardiac anomalies. This congenital abnormality involves malformation of the tricuspid valve and of the right ventricle.
Joseph, Galea +4 more
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Tachycardia in ebstein’s anomaly
Heart & Lung, 2003The patient was a 19-year-old girl with known Ebstein’s anomaly. She was on flecainide 100 mg bd for recurrent, long-standing attacks of palpitations. She presented to the emergency department during one of those attacks. The physical examination was unremarkable apart from tachycardia of 140 beats per minute.
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Echocardiography, 1993
Ebstein's anomaly, a well‐recognized congenital cardiac abnormality, involves the tricuspid valve and underlying right ventricular myocardium. The two‐dimensional diagnosis and hemodynamic characterization of this anomaly are so confident that cardiac catheterization is no longer necessary in the majority of cases.
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Ebstein's anomaly, a well‐recognized congenital cardiac abnormality, involves the tricuspid valve and underlying right ventricular myocardium. The two‐dimensional diagnosis and hemodynamic characterization of this anomaly are so confident that cardiac catheterization is no longer necessary in the majority of cases.
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