ANOMALIA DE EBSTEIN FISIOPATOLOGIA PDF

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ANOMALIA DE EBSTEIN FISIOPATOLOGIA PDF

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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A new reconstructive operation for Ebstein anomaly of the tricuspid valve. Ebstein malformation of the tricuspid valve. Am J Cardiol ; Rev Esp Cardiol [Internet]. In 2 of the 3 patients with an anomalous bundle, it could be located and sectioned during surgery. Quero Angarita, Rossi Isabel.

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Paradoxical embolization with Ebstein’s anomaly. An international co-operative study of cases. The mean follow-up lasted 4 years, and the recent echocardiograms showed good morphology of the right ventricle and tricuspid valve with mild or minimal insufficiency in 18 patients and moderate insufficiency in 2 patients.

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Abigail Simmons M, Brueckner M. A hotspot for de novo mutations causing Shprintzen-Goldberg syndrome. How to cite this article.

Complicaciones y Conducta a seguir. Ebstein Anomaly of the Tricuspid Valve.

Current knowledge about causes and inheritance. Syndromes and congenital heart defects.

Tiling path resolution mapping of constitutional 1p36 deletions by array-CGH: J Thorac Cardiovasc Surg ; Microarray analysis of 50 patients reveals the critical chromosomal regions responsible for 1p36 deletion syndrome-related complications.

Essa cirurgia foi minuciosamente descrita e publicada anomalja 5.

Atresia tricúspide

Paranon S, Acar P. Mayo Clin Proc ; Surgical treatment of Ebstein’s anomaly. Pediatr Cardiovasc Med Second Ed. J Am Coll Cardiol.

Prenatal diagnosis of Down’s syndrome in the presence of isolated Ebstein’s anomaly. Ebstein anomaly associated with left ventricular noncompaction: De novo mutations in histone modifying genes in congenital heart disease. Natural history of Ebstein’s anomaly of the tricuspid valve in childhood and adolescence: Services on Demand Journal.

Am J Hum Genet. Presentation and outcome from fetus to adult. Embryology of the heart and its impact on understanding fetal and neonatal heart disease. J Am Coll Cardiol [Internet]. A clinical case report.

FISIOPATOLOGIA DE LAS CARDIOPATIAS

Libr la salud Cardiovasc [Internet]. An autosomal dominant condition that can be caused by mutations in MYH7. Predictors of long term survival with Ebstein’s anomaly of the tricuspid valve. JavaScript is disabled for your browser. Identification of clinically relevant phenotypes in patients with Ebstein anomaly.

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Bol Asoc Med P R ; J Thorac Cardiovasc Surg. Familial ebstein anomaly, left ventricular hypertrabeculation, and ventricular septal defect associated with a MYH7 mutation. Arch Anat Physiol ; Critical Heart Disease in Infants and Children. S, Ebaid m, Zerbini EJ: Entretanto, essa sutura deve ser bem superficial.

No atrioventricular block occurred. Nora JJ, Nora ce. Br Heart J ; Ebstein’s tricuspid anomaly and Down’s syndrome.

Mosby-Year Book, ; Results of the conic reconstruction of the tricuspid valve. The technique used was efficient in repairing tricuspid insufficiency and restoring right ventricular morphology, being applicable to all anatomic types of Ebstein’s anomaly, except for Carpentier classification type D.

Emmanuilides A, Riemenschneider G.