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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Madrid A, Restrepo JP. Essa cirurgia foi minuciosamente descrita e publicada em 5. Presentation and outcome from fetus to adult.

Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy. A new reconstructive operation for Ebstein anomaly of the tricuspid valve.

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Atresia tricúspide

Paranon S, Acar P. Congenital stenosis and insufficiency of the tricuspid valve. Current knowledge about causes and inheritance. Ebstein malformation of the tricuspid valve.

Cell Mol Life Sci. Services on Demand Journal. From November to August21 patients with Ebstein’s anomaly of the tricuspid valve, with ages ranging from 20 months to 37 years mean, 23 yearsunderwent a new technique of tricuspid valvuloplasty.


J Thorac Cardiovasc Surg. From fetus to adult. Critical Heart Disease in Infants and Children. How to cite this article.

Repositorio Institucional EdocUR dc. Tiling path resolution mapping of constitutional 1p36 deletions by array-CGH: Libr la salud Cardiovasc [Internet].

CARDIOPATIAS CONGENITAS by carlos alberto de oliveira on Prezi

Am J Hum Genet. Embryology of the heart and its impact on understanding fetal and neonatal heart disease.

Appl Clin Genet [Internet]. Natural history of Ebstein’s anomaly of tricuspid valve in childhood and adolescence. Recenti Prog Med ; Fetal Diagn Ther ; To assess the results of a technical modification of tricuspid valvuloplasty in Ebstein’s anomaly.


Ebstein Anomaly of the Tricuspid Valve. Br Heart J ; This technique consisted of total or almost total detachment of the anterior tricuspid megaleaflet from the ventricular wall and valvular ring, transforming it into a cone, whose vertex remained fixed in the right ventricular tip, and the base was sutured to the tricuspid ring, after its plication, adjusting it to the size of the base of the cone tricuspid ringincluding the septal region.

Genetic heterogeneity and association with microdeletions 1p36 and 8p Eur J Hum Genet. Paradoxical embolization with Ebstein’s anomaly.

Syndromes and congenital heart defects. J Am Coll Cardiol ;