NUCHAL TRANSLUCENCY MARKER FETAL CHROMOSOME CHANGES IN THE FIRST QUARTER

• Autores: Quispe, José, Almandoz, Ángela, Q. de Michelena, María
• Formato: artículo
• Fecha de Publicación: 2015
• Institución: Sociedad Peruana de Obstetricia y Ginecología
• Repositorio: Revista Peruana de Ginecología y Obstetricia
• Lenguaje: español
• OAI Identifier: oai:ojs.pkp.sfu.ca:article/640
• Enlace del recurso: http://51.222.106.123/index.php/RPGO/article/view/640
• Nivel de acceso: acceso abierto

Objective: We evaluated the effectiveness of fetal nuchal translucency thickness measurement in routine transvaginal ultrasound screening at 10-14 gestational weeks as a predictor of Downs syndrome in the fetus. Material and methods: A total of 424 pregnant women including one with a twin pregnancy were scanned in the first trimester of pregnancy using a fixed cutoff point of 3 mm for the nuchal translucency measurement. Among these cases 64 had an amniocentesis for fetal karyotyping, other 5 fetuses miscarried spontaneously and one malformed liveborn had also a chromosome analysis. Results: The 410 cases with nuchal translucency thickness less than 3 mm resulted in 409 normal newborns and one baby trisomy 13. A nuchal translucency of 3 mm or greater was detected in 14 pregnancies with the following results: 3 normal babies, 7 with Downs syndrome, 2 with Turners syndrome and 2 were miscarried spontaneously without chromosome analysis. Conclusion: This study demonstrates that first trimester nuchal translucency combined with maternal age is an effective method of screening for fetal chromosomic abnormalities and can be used in routine clinical practice.