Results 81 to 90 of about 3,161 (171)
Ebstein’s anomaly is a rare congenital displacement of the tricuspid valve resulting in atrialization of the right ventricle. About half of the patients with Ebstein’s anomaly also have atrial septal defects, which may lead to chronic shunting and ...
Leonardo A. Marquez Roa +4 more
doaj +1 more source
Background Ebstein's anomaly and tricuspid valve dysplasia are associated with perinatal mortality approaching 50% and are among the most difficult fetal conditions to manage.
Annette Wacker‐Gussmann +4 more
doaj +1 more source
Pediatric Giant Right Atrial Aneurysm: A Case Series and Review of the Literature [PDF]
Giant right atrial aneurysm is a rare form of congenital heart disease with a wide spectrum of clinical presentation varying from asymptomatic patients to those with refractory atrial arrhythmias or severe airway obstruction.
Harder, Erika E. +3 more
core +1 more source
Himalayan P waves in COPD - A Rare Feature [PDF]
Himalayan or giant P-waves (amplitude =5 mm) are often known to be classically associated with congenital heart diseases with right to left shunt like tricuspid atresia, Ebstein anomaly, combined tricuspid and pulmonic stenosis, etc, where they indicate ...
Babu, SNM +5 more
core +1 more source
Ebstein\'s anomaly and a rare coagulation disorder – Case report and review of literature
Backgrounds: Ebstein’s anomaly of tricuspid valve is a rare congenital heart anomaly. Surgical implantation of artefi cial tricuspid valve is a standard treatment modality.
Jure Dolenc +4 more
doaj
Safety of epidural labor analgesia in a parturient with Ebstein's anomaly [PDF]
The rare congenital heart defect of Ebstein's anomaly is characterized by downward displacement and elongation of the tricuspid valve with poorly contractile right ventricle, an enlarged right atrium along with tricuspid regurgitation.
Madhura Deosthali +2 more
doaj
Isolated Biventricular Noncompaction in an adult with severe pulmonary hypertension : an association reviewed. [PDF]
Biventricular noncompaction is a recently recognized rare form of cardiomyopathy. It is characterized by altered structure of myocardial wall as a result of intrauterine arrest of compaction of the myocardial fibers in absence of coexisting congenital
Awasthy, Neeraj +2 more
core +1 more source
anomalía de Ebstein; malformación cardiaca; adulto
Introduction: Ebstein's anomaly is a rare congenital cardiac malformation, defined by an apical displacement of the septal and posterior leaflets of the tricuspid valve into the right ventricle, instead of at the level of the atrioventricular ring, which
Yvonne Y. Cárdenas Torre +1 more
doaj +2 more sources
Postoperative persistent diastolic dyssynchronous expansion in patients with Ebstein's anomaly.
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 +1 more source

