Cargando…
Prenatal diagnosis of a 46,XX male following noninvasive prenatal testing
Case report involving a normal female by NIPT with male external genitalia on routine fetal morphology assessment. QF-PCR, CGH microarray, and FISH revealed an unbalanced translocation, involving the short arms of the X and Y chromosomes. This case demonstrates the possible limitations of correctly...
Autores principales: | Mansfield, Nerida, Boogert, Tom, McLennan, Andrew |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Ltd
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4614655/ https://www.ncbi.nlm.nih.gov/pubmed/26509022 http://dx.doi.org/10.1002/ccr3.352 |
Ejemplares similares
-
Karyotyping and prenatal diagnosis of 47,XX,+ 8[67]/46,XX [13] Mosaicism: case report and literature review
por: Sun, Shaohua, et al.
Publicado: (2019) -
A case of prenatal diagnosis of 18p deletion syndrome following noninvasive prenatal testing
por: Zhao, Ganye, et al.
Publicado: (2019) -
Detection of SRY‐positive46,XX male syndrome by the analysis of cell‐free fetal DNA via non‐invasive prenatal testing
por: De Falco, Luigia, et al.
Publicado: (2019) -
Prenatal diagnosis of a de novo trisomy 20p detected by noninvasive prenatal testing
por: Yan, Xu, et al.
Publicado: (2021) -
Application of ultrasound combined with noninvasive prenatal testing in prenatal testing
por: Liu, Ci, et al.
Publicado: (2022)