impe0096p144 | Sex Differentiation, Gonads and Gynaecology, and Sex Endocrinology | IMPE2023
Loch Batista Rafael
, Inacio Marlene
, Madureira Guiomar
, Miranda Mirela
, Gomes Larissa
, Rodrigues Andresa
, Funari Mariana
, Bachega Tania
, Bilharinho Mendonca Berenice
Introduction: Congenital Adrenal Hyperplasia (CAH) is a group of autosomal recessive disorders. Defects in the 21-hydroxylase (21OH) enzyme make up 90% of CAH. These defects result in androgen excess in salt-wasting or simple virilizing forms. As androgens play a role in human psychosexual development, this study was designed to evaluate the impact of androgens on the psychosexuality of individuals with CAH due to 21OH deficiency.<strong...