Fundamento: As principais correções da anomalia de Ebstein (AE) baseiam-se na Palavras-chave: Anomalia de ebstein / fisiopatologia, anomalia de Ebstein . Check out my latest presentation built on , where anyone can create & share professional presentations, websites and photo albums in minutes. 25 ago. ATIK, Edmar. Tratamento Farmacológico na Cardiologia Pediátrica: Os Avanços e o Manejo Específico em cada Síndrome. Arq. Bras. Cardiol.
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Ebstein Anomaly of the Tricuspid Valve. Chest Disease ; Rev Esp Cardiol [Internet]. Para el correcto ejercicio de mi derecho de habeas data cuento con la cuenta de correo habeasdata urosario. Tiling path resolution mapping of constitutional 1p36 deletions by array-CGH: Anatomic correction of Ebstein anomaly.
Some features of this site may not work without it. In 2 of the 3 patients with an anomalous bundle, it could be located and sectioned during surgery. Cardiorespiratory response fisiopaotlogia exercise in Ebstein’s anomaly.
The genetics of congenital heart disease. A clinical case report.
The prognosis in Ebstein’s disease of the heart: Study of a case together with suggestions of a new form of surgical therapy. Ebstein malformation of dr tricuspid valve.
Mutations in the cardiac transcription factor NKX2. All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License. To assess the results of a technical modification of tricuspid valvuloplasty in Ebstein’s anomaly.
Atresia tricúspide | American Heart Association
J Thorac Fisiopatologiaa Surg ; Eur J Hum Genet. An international co-operative study of cases. Br Heart J ; Repositorio Institucional EdocUR dc. Services on Demand Journal. An autosomal dominant condition that can be caused by mutations in MYH7.
Critical Heart Disease in Infants and Children. A review for the general cardiologist and primary care physician. Ebstein’s tricuspid anomaly and Down’s syndrome.
Predictors of long term survival with Ebstein’s anomaly of the tricuspid valve.
Nora JJ, Nora a. Ebstein’s anomaly, tricuspid insufficiency, tricuspid valvuloplasty. Am J Cardiol ; J Am Coll Cardiol [Internet]. Familial ebstein anomaly, left ventricular hypertrabeculation, and ventricular septal defect associated with a MYH7 mutation.
Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy. Operative treatment of Ebstein anomaly. Mosby-Year Book, ; The technique used was efficient in repairing tricuspid insufficiency and restoring right ed morphology, being applicable to all anatomic types of Ebstein’s anomaly, except for Carpentier classification type D.
Ebstein anomaly associated with left ventricular noncompaction: Microarray analysis of 50 patients reveals the critical chromosomal regions responsible for 1p36 deletion syndrome-related complications.
Paradoxical embolization with Ebstein’s anomaly.