Cargando…
Karyotyping and prenatal diagnosis of 47,XX,+ 8[67]/46,XX [13] Mosaicism: case report and literature review
BACKGROUND: Trisomy 8 mosaicism has a wide phenotypic variability, ranging from mild dysmorphic features to severe malformations. This report concluded a female pregnant woman with trisomy 8 mosaicism, and carefully cytogenetic diagnoses were performed to give her prenatal diagnostic information. Th...
Autores principales: | Sun, Shaohua, Zhan, Fang, Jiang, Jiusheng, Zhang, Xuerui, Yan, Lei, Cai, Weiyi, Liu, Hailiang, Cao, Donghua |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6925423/ https://www.ncbi.nlm.nih.gov/pubmed/31864361 http://dx.doi.org/10.1186/s12920-019-0639-8 |
Ejemplares similares
-
Turner Syndrome: A Unique Mosaic Case with 45,X/47,XX,+21/46,XX Cell Lines
por: Mačkić-Đurović, Mirela, et al.
Publicado: (2018) -
A rare 47 XXY/46 XX mosaicism with clinical features of Klinefelter syndrome
por: Mohd Nor, Noor Shafina, et al.
Publicado: (2016) -
SUN-208 Rare Case of 47XXY/46XX Mosaic Klinefelter Syndrome
por: Purushothaman, Archana, et al.
Publicado: (2019) -
An Adolescent Boy with Klinefelter Syndrome and 47,XXY/46,XX Mosaicism: Case Report and Review of Literature
por: Hovnik, Tinka, et al.
Publicado: (2022) -
Rare Disorder of Sexual Differentiation with a Mosaic 46,XX/47,XXY in a Klinefelter Syndrome Individual
por: Pattamshetty, Preethi, et al.
Publicado: (2020)