46,XX DSD: Developmental, Clinical and Genetic Aspects

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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Bibliographic Details
Main Authors: Camelia Alkhzouz, Simona Bucerzan, Maria Miclaus, Andreea-Manuela Mirea, Diana Miclea
Format: Article
Language:English
Published: MDPI AG 2021-07-01
Series:Diagnostics
Subjects:
differences/disorders of sex development
46,XX
adrenal
gonad
enzymes
genetics
Online Access:https://www.mdpi.com/2075-4418/11/8/1379

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