Diagnóstico prenatal de anomalías cromosómicas Examen prenatal no invasivo

María Isabel Quiroga de Michelena; Alicia Díaz Kuan

doi:10.31403/rpgo.v62i1921

Prenatal diagnosis of chromosome abnormalities Noninvasive prenatal testing

Authors

María Isabel Quiroga de Michelena Médico Genetista, Instituto de Medicina Genética; Profesora Emérita, Universidad Peruana Cayetano Heredia
Alicia Díaz Kuan Médico Genetista, Instituto de Medicina Genética

DOI:

https://doi.org/10.31403/rpgo.v62i1921

Abstract

Non-invasive prenatal test (NIPT) is a screening method that identifies pregnant women with a high aneuploidy risk, specifically for trisomy 21, 18, 13, and chromosome X anomalies. NIPT analyzes free fetal DNA found in maternal blood. In this review, we describe the benefits, disadvantages and study indications.

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Published

2016-10-17

How to Cite

Quiroga de Michelena, M. I., & Díaz Kuan, A. (2016). Prenatal diagnosis of chromosome abnormalities Noninvasive prenatal testing. The Peruvian Journal of Gynecology and Obstetrics, 62(3), 265–268. https://doi.org/10.31403/rpgo.v62i1921

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Issue

Vol. 62 No. 3 (2016)

Section

Controversias

License

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