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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Update on Kleefstra syndrome. Early and late results in twenty patients subjected to valve replacement. Entretanto, essa sutura deve ser bem superficial.

CARDIOPATIAS CONGENITAS by carlos alberto de oliveira on Prezi

Complicaciones y Conducta a seguir. Presentation and outcome from fetus to adult.

J Thorac Cardiovasc Surg. Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy. Mayo Clin Proc ; Tiling path resolution mapping of constitutional 1p36 deletions by array-CGH: The genetics of congenital heart disease. To assess the results of a technical modification of tricuspid valvuloplasty in Ebstein’s anomaly.


J Am Coll Cardiol ; Familial ebstein anomaly, left ventricular hypertrabeculation, and ventricular septal defect associated with a MYH7 mutation.

Am J Hum Genet. Nora JJ, Nora a. Madrid A, Restrepo JP. Ebstein anomaly associated with left ventricular noncompaction: Congenital stenosis and insufficiency of the tricuspid valve. Identification of clinically relevant phenotypes in patients with Ebstein anomaly. Quero Angarita, Rossi Isabel.

Atresia tricúspide

Universidad del Rosario dc. How to cite this article. Rev Esp Cardiol [Internet].

Semin Fetal Neonatal Med [Internet]. 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. Ebstein Anomaly of the Tricuspid Valve.

Syndromes and congenital heart defects. 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 ebsteim Carpentier classification type D. Ebstein’s anomaly in a patient with Anommalia syndrome.


Ebstein’s anomaly, tricuspid insufficiency, tricuspid valvuloplasty. Ebstein’s tricuspid anomaly and Down’s syndrome.

Ebstein’s anomaly: results of the conic reconstruction of the tricuspid valve

Abigail Simmons M, Brueckner M. Uber einen sehr seltenen fall von insufficienz der valvula tricuspidalis, bedingt durch eine angeborene hochgradige missbikdung derselben.

Br Heart J ; Eur J Hum Genet. Arch Surg ; A look at ebstein anomaly. How to cite this article. Br Heart J ; A clinical case report. Microarray analysis of 50 patients reveals the critical chromosomal regions responsible for 1p36 deletion syndrome-related complications. Operative treatment of Ebstein anomaly. Ebstin Am Coll Cardiol. Mosby-Year Book, ;