Postnatal outcomes of prenatally diagnosed 45,X/46,XX
Author:
Affiliation:
1. Division of Medical Genetics; University of Washington; Seattle Washington
2. Pediatric Dermatology; Group Health Cooperative; Seattle Washington
Funder
Medical Genetics Postdoctoral Fellowship
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.37551/fullpdf
Reference15 articles.
1. Fertility and pregnancy outcome in Danish women with Turner syndrome;Birkebaek;Clin Genet,2002
2. The phenotype of 45,X/46,XY mosaicism: An analysis of 92 prenatally diagnosed cases;Chang;Am J Hum Genet,1990
3. Turner Syndrome
4. Chromosomal mosaicism mitigates stigmata and cardiovascular risk factors in Turner syndrome;El-Mansoury;Clin Endocrinol,2007
5. Pregnancy outcomes of prenatally diagnosed Turner syndrome: A French multicenter retrospective study including a series of 975 cases;Gruchy;Prenat Diagn,2014
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1. Prevalence, diagnostic features, and medical outcomes of females with Turner syndrome with a trisomy X cell line (45,X/47,XXX): Results from the InsighTS Registry;American Journal of Medical Genetics Part A;2024-07-17
2. Clinical practice guidelines for the care of girls and women with Turner syndrome;European Journal of Endocrinology;2024-05-15
3. Prenatal Findings in Postnatal Cases of Disorders of Sex Development: Experience from a Tertiary-Specialized Center in Brazil;Fetal Diagnosis and Therapy;2023-10-04
4. 45,X/46,XX at amniocentesis associated with a favorable outcome and postnatal decrease of the 45,X cell line;Taiwanese Journal of Obstetrics and Gynecology;2022-11
5. Progressive increase of the mosaic level for 45,X in 45,X/46, XX at different amniocenteses and postnatal progressive decrease of the 45,X cell line in a mosaic 45,X/46, XX fetus with a favorable outcome;Taiwanese Journal of Obstetrics and Gynecology;2022-09
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