Prenatal diagnosis of the atrioventricular septal defect and it's effect on the outcome of the pregnancies;Az atrioventricularis septumdefectus praenatalis diagnózisa és annak hatása a magzat életkilátásaira

Orvosi Hetilap

Volumn 146, Issue 34, 2005, Pages 1775-1780

  Hajdú, Júlia ^a,b   Beke, Artúr ^a   Pete, Barbara ^a   Oroszné, Nagy Judit ^a   Papp, Zoltán ^a  

^a SEMMELWEIS UNIVERSITY   (Hungary)

^b NONE   (Hungary)

Author keywords

Atrioventricular septal defect; Chromosomal anomaly; Extracardiac malformations; Prenatal diagnosis

Indexed keywords

ADULT; ARTICLE; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CONTROLLED STUDY; DIAPHRAGM HERNIA; FETUS; FETUS DEATH; GESTATIONAL AGE; HEART SEPTUM DEFECT; HUMAN; KARYOTYPE; MAJOR CLINICAL STUDY; NEWBORN DEATH; PREGNANCY OUTCOME; PREGNANCY TERMINATION; PRENATAL DIAGNOSIS; TRISOMY; TRISOMY 18; TRISOMY 21; TRISOMY 22; ADOLESCENT; EARLY DIAGNOSIS; ECHOCARDIOGRAPHY; FEMALE; GENETICS; MALE; METHODOLOGY; NEWBORN; PATHOLOGY; PREGNANCY; PROGNOSIS; RETROSPECTIVE STUDY;

ADOLESCENT; ADULT; CHROMOSOME ABERRATIONS; EARLY DIAGNOSIS; ECHOCARDIOGRAPHY; FEMALE; GESTATIONAL AGE; HEART SEPTAL DEFECTS, ATRIAL; HEART SEPTAL DEFECTS, VENTRICULAR; HUMANS; INFANT, NEWBORN; MALE; PREGNANCY; PREGNANCY OUTCOME; PRENATAL DIAGNOSIS; PROGNOSIS; RETROSPECTIVE STUDIES;

EID: 32944475422     PISSN: 00306002     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (22)

1. Allan, L. D., Sharland, G. K., Milburn, A. és mtsai: Prospective diagnosis of 1006 consecutive cases of congenital heart disease in the fetus. J. Am. Coll. Cardiol., 1994, 23, 1452-1458.
2. Allan, L. D.: Atrioventricular septal defect in the fetus. Am. J. Obstet. Gynecol., 1999, 181, 1250-1253.
3. Amark, K., Sunnegardh, J.: The effect of changing attitudes to Down's syndrome in the management of complete atrioventricular septal defects. Arch. Dis. Child. 1999, 81, 151-154.
4. Armstrong, E. J., Bischoff, J.: Heart valve development: endothelial cell signaling and differentiation. Circ. Res., 2004, 95, 459-470.
5. Boneva, R. S., Botto, L. D., Moore, C. A. és mtsai: Mortality associated with congenital heart defects in the United States: trends and racial disparities, 1979-1997. Circulation, 2001, 103, 2376-2381.
6. Brick, D. H., Allan, L. D.: Outcome of prenatally diagnosed congenital heart disease: an update. Pediatr. Cardiol., 2002, 23, 449-453.
7. Delisle, M. F., Sandor, G. G., Tessier, F. és mtsai: Outcome of fetuses diagnosed with atrioventricular septal defect. Obster. Gynecol., 1999, 94, 763-767.
8. Gelb, B. D.: Genetic basis of congenital heart disease Curr. Opin. Cardiol., 2004, 19, 110-115.
9. Hansman, M.: Trisomy 21 in mid trimester: sonographic phenotyping of the fetus is the key. Ultrasound. Obstet. Gynecol., 2004, 23, 531-534.
10. Heide, H., Thomson, J. D. R., Warton, G. A. és mtsa: Poor sensitivity of routine fetal anomaly ultrasound screening for antenatal detection of atrioventricular septal defect. Heart, 2004, 90, 916-917.
11. Hoffman, J. I. E., Kaplan, S., Liberthson, R. R.: Prevalence of congenital heart disease. Am. Heart J., 2004, 147, 425-439.
12. Lamers, W. H., Moorman, A. F. M.: Cardiac septation: a late contribution of the embryonic primary myocardium to heart morphogenesis. Circ. Res., 2002, 91, 93-103.
13. Levi, S., Montenegro, N. A.: Eurofetus: an evaluation of routine ultrasound screening for the detection of fetalé defects: aims and method. Annals of the New York Academy of Sciences, 1998, 847, 103-117.
14. Maslen, C. L.: Molecular genetics of atrioventricular septal defects. Curr. Opin. Cardiol., 2004, 19, 205-210.
15. Menahem, S., Grimwade, J.: Pregnancy termination following prenatal diagnosis of serious heart disease in the fetus. Early Hum. Dev., 2003, 73, 71-78.
16. Mirlesse, V., Cruz, A., Le Bidois, J. és mtsai: Perinatal management of fetal cardiac anomalies in a specialised obstetric-pediatric center. Am. J. Perinatol., 2001, 18, 363-371.
17. Montana, E., Khoury, M. J., Cragan, J. D. és mtsai: Trends and outcomes after prenatal diagnosis of congenital malformations by fetal echaocardiography in a well defined population, Atlanta, Georgia, 1990-1994. J. Am. Cardiol., 1996, 28, 1805-1809.
18. Reamon-Buettner, S. M., Borlak, J.: Somatic NKX2-5 mutations as a novel mechanism of disease in complex congenital heart disease. J. Med. Genetics, 2004, 41, 684-690.
19. Simpson, L. L.: Indications for fetal echocardiography from a tertiary-care obstetrics sonography practice. J. Clinic. Ultrasound, 2004, 32, 123-128.
20. Sullivan, I. D.: Prenatal diagnosis of structural heart disease: does it make a difference to survival? Arch. Dis. Child., 2002, 87F, 19-20.
21. Tabor, A., Zdravkovic, M., Perslev, A. és mtsai: Screening for congenital malformations by ultrasonography in the general population of pregnant women: factors affecting the efficacy. Acta Obstet. Gynecol. Scand., 2003, 82, 1092-1098.
22. Tordos T.: Prenatal diagnosis and management of fetal cardiovascular malformations. Curr. Opin. Obstet. Gynecol., 2000, 12, 105-109.