NHẬN XÉT KẾT QUẢ CHẨN ĐOÁN TRƯỚC SINH HỘI CHỨNG TURNER TẠI BỆNH VIỆN PHỤ SẢN HÀ NỘI
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#Hội chứng turner #Khảm #Karyotype #Bất thường siêu âm #Chẩn đoán trước sinhTài liệu tham khảo
Baena N, Vigan CD, Cariati E, et al. Turner syndrome: Evaluation of prenatal diagnosis in 19 European. Am J Med Genet A. 2004; 129A(1):16-20.
Kaisenberg CS, Wilting J, Dörk T, et al. Lymphatic capillary hypoplasia in the skin of fetuses with increased nuchal translucency and Turner’s syndrome: Comparison with trisomies and controls. Mol Hum Reprod. 2010; 16(10):778-789.
Csaba P, Artur B, Gabor M, et al. Prenatal diagnosis of turner syndrome: Report on 69 cases. J Ultrasound Med. 2006; 25(6):711-717.
Louise K, Ricardo PD, Debbie N, et al. Non-invasive prenatal testing for sex chromosome aneuploidy in routine clinical practice. Fetal Diagn Ther. 2018; 44(2):85-90.
Bing H, Maya T, Sucheta B, et al. Prenatal diagnosis of 45,X and 45,X mosaicism: The need for thorough cytogenetic and clinical evaluations. Prenat Diagn. 2002; 22(2):105-110.
Allybocus ZA. Clinical significance of ultrasonography markers in prenatal diagnosis of turner syndrome in fetuses-90 cases reports. J Radiol Clin Imaging. 2019:7-15.
Claus HG, Niels HA, Gerard SC, et al. Clinical practice guidelines for the care of girls and women with Turner syndrome: Proceedings from the 2016 Cincinnati International Turner Syndrome Meeting. Eur J Endocrinol. 2017; 177(3):G1-G70.
Sybert VP. Phenotypic effects of mosaicism for a 47,XXX cell line in Turner syndrome. J Med Genet. 2002; 39(3):217-220.