ANOMALIA DE EBSTEIN PRENATAL PDF

Leite; Roberto B. Gianisella; Paulo Zielinsky. Nos dois casos restantes a anomalia de Ebstein foi descoberta na idade adulta, aos 55 anos 7 e durante necropsia 5. Ebstein W. Uber einen sehr seltenen fall von insufficienz der valvula tricuspidalis, bedingt durch eine angeborene hochgradige missbikdung derselben.

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Leite; Roberto B. Gianisella; Paulo Zielinsky. Nos dois casos restantes a anomalia de Ebstein foi descoberta na idade adulta, aos 55 anos 7 e durante necropsia 5. Ebstein W. Uber einen sehr seltenen fall von insufficienz der valvula tricuspidalis, bedingt durch eine angeborene hochgradige missbikdung derselben.

Arch Anat Physiol ; Apud : Epstein ML. Congenital stenosis and insufficiency of the tricuspid valve. In: Emmanuilides A, Riemenschneider G. Epstein ML. Moss and Adams. Heart Disease in Infants Children and Adolescents. Ebstein's anomaly. In: Nichols DG. Critical Heart Disease in Infants and Children. St Louis: Mosby-Year Book, Watson H. Natural history of Ebstein's anomaly of tricuspid valve in childhood and adolescence.

An international co-operative study of cases. Br Heart J ; Ebstein's anomaly in a patient with Down's syndrome. Prenatal diagnosis of Down's syndrome in the presence of isolated Ebstein's anomaly. Fetal Diagn Ther ; Ebstein's tricuspid anomaly and Down's syndrome. A clinical case report. Recenti Prog Med ; Syndromes and congenital heart defects. Louis: Mosby-Year Book, ; Mair DD. Ebstein's anomaly: natural history and management. J Am Coll Cardiol ; All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License.

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2014, Número 02

Ebstein's anomaly is a rare complex congenital heart defect of the tricuspid valve. We aimed to describe the frequency, clinical profile, and early and short-term post-operative results in patients under the age of 18 years operated for this anomaly in a tertiary center in Angola.. A retrospective cross-sectional study was conducted over a period of 37 months. We analyzed all patients diagnosed with congenital heart defects.. Of the patients studied, eight 0. Mean cardiothoracic index was 0. Seven patients

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2013, Número 05

There is no recognized gender predilection, and almost all cases seem to be sporadic, although an association with maternal lithium carbonate injection has been postulated 6. A few familial cases have been reported 6,7. In less severe cases, it may present at birth. Depending on the degree of atrial right-to-left shunting , the infant may or may not be cyanotic. The main abnormality is an abnormal tricuspid valve particularly septal and posterior leaflets , which is displaced apically into the right ventricle , resulting in atrialization of the parts of the ventricle above the valve.

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A review. Mayo Clin Proc , Arch Inst Cardiol Mex ; J Am Coll Cardiol ;

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