Fetal cardiology. Fetal Echocardiography Prenatal Diagnostic anomalía de Ebstein fetal cardiología fetal diagnóstico prenatal ecocardiografía fetal; Language of. A case of prenatal diagnosis of Ebstein’s anomaly in a Anomalia de Ebstein detectada in utero e síndrome de Down: diagnóstico pré-natal. PDF | Ebstein’s anomaly is an uncommon congenital heart defect, with a Anomalia de Ebstein Com Valva Tricúspide Imperfurada.

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Follow-up was in the first half of Junewhen all patients underwent clinical, radiological and echocardiography assessment. Pedigree analysis indicated that CTVM segregated as an autosomal dominant trait with reduced penetrance. Nonsyndromic Ebstein anomaly can occur as a sporadic or a familial defect summary by Digilio et al.

All patients were operated: Ebstein’s tricuspid anomaly and Down’s syndrome. Genomewide linkage analysis in 1 kindred identified a CTVM susceptibility locus on chromosome 9 with a maximum multipoint lod score of 3.

How to cite this article. Expert curators review the literature and organize it to facilitate your work. Mosby-Year Book, ; Associated deformity of the tricuspid leaflets and defect of the atrial septum are frequent.

A clinical case report. We analysed echocardiographic parameters and its correlation with the perinatal development of 16 cases diagnosed with Ebstein’s anomaly.


Diagnóstico y pronóstico fetales de la anomalía de Ebstein.

Looking For More References? The indications for surgery were: An international ebsetin study of cases. Cardiothoracic index, echocardiographic findings, surgical indications, surgery performed and early post-operative evaluation.

Cavopulmonary shunt was reserved for patients less than six months old and for those with significant RV dysfunction. Se continuar a navegar, consideramos que aceita o seu uso. In 2 unrelated patients with Ebstein anomaly and other malformations, de Lonlay-Debeney et al. Fetal echocardiography is possible to confirm with great certainty the diagnosis, in utero, Ebstein’s anomaly, as well as determine its perinatal prognosis.

Secondary repair of Ebstein’s anomaly with atrioventricular septal defect using the cone technique. Of the patients studied, eight 0.

Ebstein’s anomaly in children: A single-center study in Angola | Revista Portuguesa de Cardiologia

No patients with a genetic syndrome or WPW syndrome were found. Cardiol Young, 14pp. Cardiol Young, 16pp. CC ]. Mean cardiothoracic index decreased to 0. The same combination of Ebstein anomaly in 1 sib and comparable mitral anomaly in another was apparently present in the family reported by Yamauchi and Cayler Ebstein anomaly is characterized by downward displacement of variable severity of the tricuspid valve into the right ventricle.

Follow-up was in the first half of Junewhen all patients underwent clinical, radiological and echocardiography assessment. Several techniques have been described to avoid this complication.


A new reconstructive operation for Ebstein’s anomaly of the tricuspid valve. The mean follow-up was 1.

Bol Asoc Med P Ptenatal ; Although associations between EA and certain genetic syndromes have been described, mainly trisomy 21 and WPW syndrome, 9,14 these syndromes were not found in the present series. Ebstein’s anomaly in children: In 28 patients with nonsyndromic Ebstein anomaly, Digilio et al. Demographic data, clinical presentations, and NYHA functional class of the study population are shown in Table 1.

Am J Med Genet A,pp. However, the technique could not be applied in two patients for the reasons described above. Natural history of Ebstein’s anomaly of tricuspid valve in childhood and adolescence.

The authors declare that they have followed the protocols of their work center on the publication of anomaila data. We need long-term secure funding to provide you the information that you need at your fingertips. Evolution of cardiothoracic index in the five patients undergoing cone reconstruction. Arch Anat Physiol ;