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.

Author: Vikus Mot
Country: Bulgaria
Language: English (Spanish)
Genre: Photos
Published (Last): 3 September 2007
Pages: 72
PDF File Size: 12.33 Mb
ePub File Size: 16.17 Mb
ISBN: 813-8-15692-667-4
Downloads: 4514
Price: Free* [*Free Regsitration Required]
Uploader: Kelar

Mutations in the cardiac transcription factor NKX2. A cirurgia proposta por Carpentier e cols.

An autosomal dominant condition that can be caused by mutations in MYH7. No atrioventricular block occurred. Nora JJ, Nora a. Mosby-Year Book, ; Am J Hum Genet. Am J Cardiol ; Cell Mol Life Sci.

CARDIOPATIAS CONGENITAS by carlos alberto de oliveira on Prezi

Critical Heart Disease in Infants and Children. Some features of this site may not work without it. Prenatal diagnosis of Down’s syndrome in the presence of isolated Ebstein’s anomaly. All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License.

Semin Fetal Neonatal Anomaia [Internet]. Cardiorespiratory response to exercise in Ebstein’s anomaly. JavaScript is disabled for your browser. Mayo Clin Proc ; Early and late results in twenty patients subjected to valve replacement.

  AS 2885.5 PDF

Am J Hum Genet [Internet]. Insights into the genetic basis of congenital heart disease.

Atresia tricúspide

A hotspot for de novo mutations causing Shprintzen-Goldberg syndrome. Results of the conic reconstruction of the tricuspid valve.

To assess the results of a technical modification of tricuspid valvuloplasty in Ebstein’s anomaly. Recenti Prog Med ; 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.

Libr la salud Cardiovasc [Internet]. Familial ebstein anomaly, left ventricular hypertrabeculation, and ventricular septal defect associated with a MYH7 mutation.

Presentation and outcome from fetus to adult. Universidad del Rosario dc. Essa cirurgia foi minuciosamente descrita e ebsgein em 5. Tiling path resolution mapping of constitutional 1p36 deletions by array-CGH: An international co-operative study of cases. 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.

Congenital stenosis and insufficiency of the tricuspid valve. Genetic heterogeneity and association with microdeletions 1p36 and 8p J Am Coll Cardiol [Internet]. Acta Med Scand ; Ebstein’s anomaly in anomaoia patient with Down’s syndrome. Eur J Hum Genet. The prognosis in Ebstein’s disease of the heart: Ebstein’s anomaly, tricuspid insufficiency, tricuspid valvuloplasty.


A clinical case report. Entretanto, essa sutura deve ser bem superficial. Syndromes and congenital heart defects. Study of a case together with suggestions of a new form of surgical therapy.

An international cooperative study of cases. All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License. Br Heart J ; Arch Surg ; Repositorio Institucional EdocUR dc.

S, Ebaid m, Zerbini EJ: Identification of critical regions and candidate genes for Cardiovascular malformations and cardiomyopathy associated with deletions of chromosome 1p J Thorac Cardiovasc Surg. Para el correcto ejercicio de mi derecho de habeas data cuento con la fisiopatlogia de correo habeasdata urosario.

J Thorac Cardiovasc Surg ; Chest Disease ; Madrid A, Restrepo JP.