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Clinical characteristics and prenatal diagnosis of fetuses with sex chromosomal aneuploidies detected by non-invasive prenatal testing during early and midterm pregnancies / 中华医学遗传学杂志
Chinese Journal of Medical Genetics ; (6): 321-324, 2021.
Article Dans Chinois | WPRIM | ID: wpr-879577
ABSTRACT
OBJECTIVE@#To analyze the indication, karyotyping result, ultrasound finding, pregnancy decision and follow-up of fetuses with sex chromosome aneuploidies (SCA) detected by non-invasive prenatal testing (NIPT) during early and midterm pregnancies.@*METHODS@#The results of 225 singleton pregnancies with fetal SCA detected by NIPT were reviewed and analyzed.@*RESULTS@#The 225 cases included 45,X (n=37), 47,XXY (n=74), 47,XXX (n=50), 47,XYY (n=56) and mosaicisms (n=8), among which 121 (53.8%) have opted to terminate the pregnancy, including 45,X (n=31), 47,XXY (n=61), 47,XXX (n=14), 47,XYY (n=12) and 3 mosaicisms. The remainder 104 (46.2%) have elected to continue with the pregnancy, among which three have opted to terminate due to abnormalities detected by ultrasonography, and two had spontaneous abortions.@*CONCLUSION@#NIPT as a first-tier screening method can effectively detect fetal trisomies 21, 13 and 18 as well as SCA. The types of fetal SCA and presence of ultrasound abnormalities are critical factors for the termination of pregnancy.
Sujets)
Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Diagnostic prénatal / Aberrations des chromosomes sexuels / Trisomie / Syndrome de Down / Foetus / Aneuploïdie Type d'étude: Etude diagnostique / Étude pronostique Limites du sujet: Femelle / Humains / Grossesse langue: Chinois Texte intégral: Chinese Journal of Medical Genetics Année: 2021 Type: Article

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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Diagnostic prénatal / Aberrations des chromosomes sexuels / Trisomie / Syndrome de Down / Foetus / Aneuploïdie Type d'étude: Etude diagnostique / Étude pronostique Limites du sujet: Femelle / Humains / Grossesse langue: Chinois Texte intégral: Chinese Journal of Medical Genetics Année: 2021 Type: Article