46,XX DSD: Developmental, Clinical and Genetic Aspects

Differences in sex development (DSD) in patients with 46,XX karyotype occur by foetal or postnatal exposure to an increased amount of androgens. These disorders are usually diagnosed at birth, in newborns with abnormal genitalia, or later, due to postnatal virilization, usually at puberty. Proper di...

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Detalles Bibliográficos
Autores principales: Alkhzouz, Camelia, Bucerzan, Simona, Miclaus, Maria, Mirea, Andreea-Manuela, Miclea, Diana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8392837/
https://www.ncbi.nlm.nih.gov/pubmed/34441313
http://dx.doi.org/10.3390/diagnostics11081379

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8392837/
https://www.ncbi.nlm.nih.gov/pubmed/34441313
http://dx.doi.org/10.3390/diagnostics11081379

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