Results 41 to 50 of about 239,154 (181)

Successful ablation of coexistent Mahaim tachycardia and right posterior accessory pathway in a patient with Ebstein's anomaly

Türk Kardiyoloji Derneği Arşivi, 2016
Summary– The atriofascicular accessory pathway (AP), known as the Mahaim pathway, is a rare form of pre-excitation, comprising less than 3% of all APs.
Enes Elvin Gül, Celal Akdeniz, Volkan Tuzcu   +2 more
doaj   +1 more source

The Two Anomalies of Wilhelm Ebstein [PDF]

Texas Heart Institute Journal, 2017
The year 2016 was the 180th anniversary of Wilhelm Ebstein's birth and the 150th anniversary of his description of the congenital tricuspid valve malformation that came to be known as Ebstein anomaly. We present a brief history of the life and work of Dr. Wilhelm Ebstein. Despite his distinguished career, he is seemingly forgotten in his own birthplace.
Mazurak, Magdalena, Kusa, Jacek
openaire   +3 more sources

Ebstein's anomaly may be caused by mutations in the sarcomere protein gene MYH7 [PDF]

, 2011
Ebstein's anomaly is a rare congenital heart malformation characterised by adherence of the septal and posterior leaflets of the tricuspid valve to the underlying myocardium.
Moorman, A.F.M., van de Meerakker, J. B A, Keavney, B., J. W. Roos-Hesselink, Postma, A. V., van de Meerakker, J. B. A., Mulder, B., Mulder, B.J., Rahman, T., A. F. M. Moorman, A. T. J. M. Helderman-van den Enden, Roos-Hesselink, J. W., Sels, J., van de Meerakker, JBA, Mulder, B. J. M., Klaassen, S, Baars, M.J.H., Engelen, K. van, B. J. M. Mulder, B. Keavney, Sperling, S. R., Mulder, B.J.M., Sels, J-W, M. J. H. Baars, Keavney, B, Vliegen, H.W., Goodship, J., Vliegen, H., Moorman, A. F. M., Rahman, T, U. Bauer, Helderman-van d Enden, ATJM, Sels, JW, Vliegen, H. W., Helderman-van den Enden, A., Helderman-Van den Enden, A. T J M, Baars, M., S. Klaassen, Sels, J.W., Helderman-van den Enden, A.T.J.M., Klaassen, S., Baars, M. J H, Moorman, A. F M, S. R. Sperling, Mulder, BJM, Roos-Hesselink, J.W., Meerakker, J.B.A. van de, Sperling, SR, T. Pickardt, Postma, A., Roos - Hesselink, Jolien; id_orcid, van Engelen, K., Moorman, A., Pickardt, T., J. Goodship, K. van Engelen, Goodship, J, Sels, J. W., T. Rahman, Mulder, B. J M, J. B. A. van de Meerakker, Engelen, K, Moorman, AFM, J-W Sels, Bauer, U, Postma, A.V., van de Meerakker, J.B.A., H. W. Vliegen, Sperling, S., Sperling, S.R., Bauer, U., Vliegen, HW, Helderman-van den Enden, A. T. J. M., A. V. Postma, Postma, AV, Pickardt, T, Baars, MJH, Baars, M. J. H., Roos-Hesselink, J., van de Meerakker, J.   +79 more
core   +4 more sources

Incidental Finding of Ebstein's Anomaly in an Adolescent with an Upper Respiratory Infection: A Case Report [PDF]

Journal of Clinical and Diagnostic Research, 2016
Ebstein’s anomaly is a rare congenital heart disorder and has a varied clinical course, with detection as late as the seventh decade. We hereby describe an 11-year-old child in whom Ebstein’s anomaly was diagnosed.
Rohit Kapoor, Premila Paul, Premchand Anne   +2 more
doaj   +1 more source

Image to Fit the Clinical Picture: Point-of-care Ultrasound Assessment of Ebstein’s Anomaly in Peru

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, Andrea Dreyfuss, Roberto Inga   +2 more
doaj   +1 more source

Cor triatriatum dexter masquerading as Ebstein's anomaly

, 2011
We report the case of a child with cor triatriatum dexter masquerading as Ebstein's anomaly on transthoracic echocardiography. This was attributed to a floppy membrane arising from the right atrium, protruding into the tricuspid valve and pushing the ...
Souheir Salam, Orhan Uzun, David Gallacher   +2 more
core   +1 more source

Ebstein’s Anomaly, Left Ventricular Noncompaction, and Sudden Cardiac Death

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, Luke Warner, Nicholas Collins   +2 more
doaj   +1 more source

Transplacental Flecainide and/or Digoxin for Fetal Tachyarrhythmias: Therapeutic Efficacy and Clinical Experience

Prenatal Diagnosis, EarlyView.
ABSTRACT Objective To assess the efficacy and safety of transplacental flecainide and/or digoxin for fetal tachyarrhythmias when sotalol is unavailable. Method We evaluated transplacental flecainide, digoxin, or combination therapy in a retrospective and prospective cohort across two Thai tertiary centers.
Mukpradab Darakamas, Sanitra Anuwutnavin, Fuanglada Tongprasert, Wisit Chankhunaphas, Kanyarat Nilto, Supaluck Kanjanauthai, Jarupim Soongswang   +6 more
wiley   +1 more source

Rare loss-of-function variants in matrisome genes are enriched in Ebstein’s anomaly

HGG Advances
Summary: Ebstein’s anomaly, a rare congenital heart disease, is distinguished by the failure of embryological delamination of the tricuspid valve leaflets from the underlying primitive right ventricle myocardium. Gaining insight into the genetic basis of
Zhou Zhou, Xia Tang, Wen Chen, Qianlong Chen, Bo Ye, Angad S. Johar, Iftikhar J. Kullo, Keyue Ding   +7 more
doaj   +1 more source

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, Jean-Bernard Selly, Gilbert Dubois, Bernard Kreitmann, Yael Levy   +4 more
doaj   +1 more source