Cargando…
NR5A1 is a novel disease gene for 46,XX testicular and ovotesticular disorders of sex development
PURPOSE: We aimed to identify the genetic cause in a cohort of 11 unrelated cases and two sisters with 46,XX SRY-negative (ovo)testicular disorders of sex development (DSD). METHODS: Whole-exome sequencing (n = 9), targeted resequencing (n = 4), and haplotyping were performed. Immunohistochemistry o...
Autores principales: | Baetens, Dorien, Stoop, Hans, Peelman, Frank, Todeschini, Anne-Laure, Rosseel, Toon, Coppieters, Frauke, Veitia, Reiner A., Looijenga, Leendert H.J., De Baere, Elfride, Cools, Martine |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5392598/ https://www.ncbi.nlm.nih.gov/pubmed/27490115 http://dx.doi.org/10.1038/gim.2016.118 |
Ejemplares similares
-
A rare case of 46XX ovotesticular disorder of sex development
por: Reddy, Sagar S.L., et al.
Publicado: (2020) -
Steroidogenic Factor-1 (SF-1, NR5A1) and 46,XX Ovotesticular Disorders of Sex Development: One Factor, Many Phenotypes
por: McElreavey, Kenneth, et al.
Publicado: (2017) -
46, XX Ovotesticular disorder of sex development (true hermaphroditism) with seminoma: A case report
por: Li, Zixiang, et al.
Publicado: (2020) -
Antisense Oligonucleotide-Based Downregulation of the G56R Pathogenic Variant Causing NR2E3-Associated Autosomal Dominant Retinitis Pigmentosa
por: Naessens, Sarah, et al.
Publicado: (2019) -
46,XX ovotesticular disorder in a Mexican patient with Beckwith–Wiedemann syndrome: a case report
por: Macías-Gómez, Nelly Margarita, et al.
Publicado: (2012)