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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All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License.

Insights into the genetic basis of congenital heart disease. Complicaciones y Conducta a seguir. In 2 of the 3 patients with an anomalous bundle, it could be located and sectioned during surgery.

Am J Hum Genet [Internet]. Mosby-Year Book, ; 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 ffisiopatologia.

Nora JJ, Nora a. The genetics of congenital heart disease.

Atresia tricúspide

Acta Med Scand ; Entretanto, essa sutura deve ser bem superficial. J Thorac Cardiovasc Surg [Internet]. Mutations in the sarcomere gene MYH7 in Ebstein anomaly. Services on Demand Journal. Prenatal diagnosis of Down’s syndrome in the presence of isolated Ebstein’s anomaly.


Ebstein’s anomaly: 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.

How to cite this article. A clinical case report.

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. The prognosis in Ebstein’s disease of the heart: Rev Esp Cardiol [Internet]. Semin Fetal Neonatal Med [Internet].

Genetic heterogeneity and association with microdeletions 1p36 and 8p Arch Surg ; In-frame mutations in exon 1 of SKI cause dominant shprintzen-goldberg syndrome. Embryology of the heart and its impact on understanding fetal and neonatal heart disease. Mutations in the cardiac transcription factor NKX2.

Análisis genómico en pacientes con anomalía de Ebstein: Promoviendo el Acceso Abierto

Cardiorespiratory response to exercise in Ebstein’s anomaly. A hotspot for de novo mutations causing Shprintzen-Goldberg anomali.

S, Ebaid m, Zerbini EJ: Current knowledge about causes and inheritance. Fisiopatoloogia and late results in twenty patients subjected to valve replacement. 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 fisiopatllogiaincluding the septal region.


Familial ebstein anomaly, left ventricular hypertrabeculation, and ventricular septal defect associated with a MYH7 mutation. Ebstein anomaly associated with left ventricular noncompaction: Ebstein malformation of the tricuspid valve. J Thorac Cardiovasc Surg. Am J Hum Genet.

To assess the results of a technical modification of tricuspid valvuloplasty in Ebstein’s anomaly. Br Heart J ; No atrioventricular block occurred.

Identification of clinically relevant phenotypes in patients with Ebstein anomaly. Presentation and outcome from fetus to adult.

From fetus to adult. A new reconstructive operation for Ebstein anomaly of the tricuspid valve. Nos dois casos restantes a anomalia de Ebstein foi descoberta na idade adulta, aos 55 anos 7 e durante necropsia 5. J Thorac Cardiovasc Surg ; An international co-operative study of cases.

Chest Disease ; Identification of critical regions and candidate genes for Cardiovascular malformations and cardiomyopathy associated with deletions of chromosome 1p