Results 31 to 40 of about 200,194 (156)
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 +2 more
doaj +1 more source
Subarachnoid Block in a Patient with Ebstein’s Anomaly Posted for Total Abdominal Hysterectomy [PDF]
, 2021 Ebstein’s anomaly is considered to be one of the rare congenital heart conditions which occur due to abnormal development of tricuspid valve and atrialisation of right ventricle and could be associated with either Atrial Septal Defect (ASD) or Patent ...
Venkata Suryanarayana Gopavajhula +2 more
core +1 more source
Primary Tricuspid Regurgitation in ACHD: Diagnosis and Treatment
Methodist DeBakey Cardiovascular JournalPrimary tricuspid valve regurgitation includes congenital and acquired disorders, especially Ebstein anomaly and tricuspid valve dysplasia. Severe tricuspid regurgitation causes progressive right atrial and ventricular dilation, arrhythmias, exercise ...
Luciana Da Fonseca Da Silva
doaj +1 more source
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 +2 more
doaj +1 more source
, 2016 Diagnosis and management of Ebstein’s anomaly are discussed.
Bernard J. Gersh +2 more
core +1 more source
, 2018 Ebstein’s anomaly has a very varied presentation and is compatible with long-term survival. Surgical repair is now very promising and will encourage earlier intervention. Arrhythmia is a long-term concern and can be difficult to manage.
Sachin Khambadkone
core +1 more source
Prenatal Sonographic Detection of Ebstein’s Anomaly
, 2017 Ebstein’s anomaly is a rare type of congenital heart defect characterized by a malformation of the tricuspid valve and the right side of the heart. This case study presents a well-documented case of Ebstein’s anomaly that was diagnosed prenatally using ...
Kelsy L. Fisher, Mariah C. Root
core +1 more source
A “congenitally corrected” variant of Ebstein’s anomaly
, 2018 Ebstein’s anomaly is a rare CHD that is characterised by caudal displacement of the functional tricuspid annulus and a dysfunctional tricuspid valve owing to a failure of proper leaflet coaptation.
Tolga S. Güvenç +2 more
core +1 more source
, 2007 EBSTEIN’S ANOMALY IS A RARE congenital heart defect characterized by displacement of the tricuspid valve leaflets into the right ventricle.1The defect was first described by Wilhelm Ebstein in 1866.2This anomaly of the tricuspid valve causes the right ...
Sarah Pashia
core +1 more source
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 +6 more
wiley +1 more source