46,XX DSD due to Androgen Excess in Monogenic Disorders of Steroidogenesis: Genetic, Biochemical, and Clinical Features

46,XX DSD due to Androgen Excess in Monogenic Disorders of Steroidogenesis: Genetic, Biochemical, and Clinical Features

The term ‘differences of sex development’ (DSD) refers to a group of congenital conditions that are associated with atypical development of chromosomal, gonadal, or anatomical sex. Disorders of steroidogenesis comprise autosomal recessive conditions that affect adrenal and gonada...

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Bibliographic Details
Main Authors: Federico Baronio, Rita Ortolano, Soara Menabò, Alessandra Cassio, Lilia Baldazzi, Valeria Di Natale, Giacomo Tonti, Benedetta Vestrucci, Antonio Balsamo
Format: Article
Language:English
Published: MDPI AG 2019-09-01
Series:International Journal of Molecular Sciences
Subjects:
46,XX DSD
21-hydroxylase deficiency
11-hydroxylase deficiency
3β-hydroxysteroid dehydrogenase deficiency
aromatase deficiency
POR deficiency
androgen excess
Online Access:https://www.mdpi.com/1422-0067/20/18/4605

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https://www.mdpi.com/1422-0067/20/18/4605

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