Results 11 to 20 of about 3,876 (224)
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.
A. F. M. Moorman +16 more
core +4 more sources
Repair of Ebstein's Anomaly [PDF]
The Annals of Thoracic Surgery, 2004 Ebstein’s anomaly is a tricuspid valve anomaly associated with poor right ventricular contractility in severe cases. Surgery is indicated in all symptomatic patients. Tricuspid valve repair is possible in most of the cases with mobilization of the anterior leaflet and longitudinal plication of the atrialized chamber.
openaire +3 more sources
, 1994 ESCOLA PAULISTA MED,RUA BOTUCATU 740-3,BR-04023900 São Paulo,BRAZILESCOLA PAULISTA MED,RUA BOTUCATU 740-3,BR-04023900 São Paulo,BRAZILWeb of ...
Mari, J. D., Smith, MCD, Turecki, G.
core +1 more source
An Unusual Case of Tricuspid Stenosis [PDF]
, 2018 Tricuspid stenosis is an uncommon valvular abnormality commonly associated with other valvular lesions. Ebstein's anomaly is a rare congenital heart malformation characterized primarily by abnormalities of the tricuspid valve and right ventricle ...
Almeida, Jorge +6 more
core +2 more sources
Human gene copy number spectra analysis in congenital heart malformations [PDF]
, 2012 The clinical significance of copy number variants (CNVs) in congenital heart disease (CHD) continues to be a challenge. Although CNVs including genes can confer disease risk, relationships between gene dosage and phenotype are still being defined.
Bick, David P. +13 more
core +2 more sources
Neonatal Cyanosis: Diagnostic and Management Challenges [PDF]
, 2011 Neonatal central cyanosis is always a sign of serious pathological processes and may involve diverse organs and impose a significant diagnostic and therapeutic challenge.
Izraelit, A. +3 more
core +3 more sources
Management of Ebstein’s anomaly [PDF]
Annals of Cardiothoracic Surgery, 2017 Ebstein malformation is a rare disease that presents with a spectrum of severity. We use a management paradigm that breaks the anomaly into two groups: neonates and children/adults. This leads to a discussion of management and operative techniques as well as pitfalls.
Mark E. Roeser, Irving L. Kron
openaire +3 more sources
Maladie d’Ebstein : A propos d’un cas au Centre Hospitalier Universitaire de Libreville: Ebstein's anomaly: A case report at Libreville University Hospital Center [PDF]
, 2021 La maladie d’Ebstein est une cardiopathie congénitale rare. Elle est caractérisée par l’insertion basse d’un ou deux feuillets de la valve tricuspide conduisant à une atrialisation du ventricule droit.
Alakoua , Lidwine Cajole Ndjibah +4 more
core +1 more source
Management and outcome of Ebstein's anomaly in children [PDF]
, 2017 Objectives To assess clinical presentation, treatment, and outcome of children with Ebstein's anomaly. Background Data on long-term outcome of children with Ebstein's anomaly are scarce.
Attenhofer Jost, Christine H. +8 more
core
Catheterization and Cardiovascular Interventions, EarlyView.ABSTRACT We present a 74‐year‐old female with a history of mechanical aortic and mitral valve implantation and non‐Hodgkin lymphoma. She presented with right sided heart failure due to severe functional tricuspid regurgitation and was treated with transcatheter TricValve bicaval system implantation.
Marcel A. Beijk +2 more
wiley +1 more source