Cargando…
The Natural History of a Man With Ovotesticular 46,XX DSD Caused by a Novel 3-Mb 15q26.2 Deletion Containing NR2F2 Gene
Gonadal sex determination is a complex genetic process by which an embryonic primordium is driven to form an ovary or a testis, which requires a delicate dosage balance involving many genes. Disruption in this molecular pathway can lead to differences of sex development (DSD). Although some genetic...
Autores principales: | Carvalheira, Gianna, Malinverni, Andrea M, Moysés-Oliveira, Mariana, Ueta, Renata, Cardili, Leonardo, Monteagudo, Patrícia, Mathez, Andreia L G, Verreschi, Ieda T, Maluf, Miguel A, Shida, Márcia E F, Leite, Mila T C, Mazzotti, Diego, Melaragno, Maria Isabel, Dias-da-Silva, Magnus R |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Endocrine Society
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6821239/ https://www.ncbi.nlm.nih.gov/pubmed/31687637 http://dx.doi.org/10.1210/js.2019-00241 |
Ejemplares similares
-
CORRIGENDUM FOR “The Natural History of a Man With Ovotesticular 46,XX DSD Due to a Novel 3-Mb 15q26.2 Deletion Containing NR2F2 Gene”
Publicado: (2020) -
THU189 Complex Treatment Of Recurrent Gynecomastia In An Affirmed Male With 46XX Ovotesticular Difference Of Sexual Differentiation (DSD).
por: Jumani, Sanjay, et al.
Publicado: (2023) -
An ovulating follicle presenting as a testicular mass in a teenage patient with ovotesticular DSD
por: Roth, Joshua D., et al.
Publicado: (2018) -
A Novel WT1 Mutation Identified in a 46,XX Testicular/Ovotesticular DSD Patient Results in the Retention of Intron 9
por: Sirokha, Dmytro, et al.
Publicado: (2021) -
Leydig Cell Tumor in a Patient with 46,XX Disorder of Sex Development (DSD), Ovotesticular: A Case Report and a Review of the Literature
por: Gretser, Steffen, et al.
Publicado: (2021)