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Ann Endocrinol (Paris) ; 83(3): 181-185, 2022 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-35489415

RESUMO

21-Hydroxylase deficiency (21OHD) is the most common cause of congenital adrenal hyperplasia. Increased production of adrenal-derived androgens and progesterone in 21OHD women interfere with their reproductive function and their fertility in many different ways, depending on the severity of the disease. Sexuality and fertility in women with classic 21OHD is impaired, due to several issues such as disrupted gonadotropic axis due to androgen and progesterone overproduction, and mechanical, psychological factors related to genital surgery. Fertility and fecundity in these women get better over the years. Subfertility seems contrariwise to be relative in non-classic 21OHD women. Before pregnancy, genotyping the partner and genetic counselling is mandatory.


Assuntos
Hiperplasia Suprarrenal Congênita , Gonadotrofos , Hiperplasia Suprarrenal Congênita/complicações , Hiperplasia Suprarrenal Congênita/genética , Androgênios , Feminino , Fertilidade , Humanos , Gravidez , Progesterona , Esteroide 21-Hidroxilase/genética
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