Classic genetic and hormonal switches during fetal sex development and beyond.
Journal
Medizinische Genetik : Mitteilungsblatt des Berufsverbandes Medizinische Genetik e.V
ISSN: 1863-5490
Titre abrégé: Med Genet
Pays: Germany
ID NLM: 9440651
Informations de publication
Date de publication:
Sep 2023
Sep 2023
Historique:
pmc-release:
16
08
2024
medline:
6
6
2024
pubmed:
6
6
2024
entrez:
6
6
2024
Statut:
epublish
Résumé
Critical genetic and hormonal switches characterize fetal sex development in humans. They are decisive for gonadal sex determination and subsequent differentiation of the genital and somatic sex phenotype. Only at the first glace these switches seem to behave like the dual 0 and 1 system in computer sciences and lead invariably to either typically male or female phenotypes. More recent data indicate that this model is insufficient. In addition, in case of distinct mutations, many of these switches may act variably, causing a functional continuum of alterations of gene functions and -dosages, enzymatic activities, sex hormone levels, and sex hormone sensitivity, giving rise to a broad clinical spectrum of biological differences of sex development (DSD) and potentially diversity of genital and somatic sex phenotypes. The gonadal anlage is initially a bipotential organ that can develop either into a testis or an ovary.
Identifiants
pubmed: 38840820
doi: 10.1515/medgen-2023-2036
pii: medgen-2023-2036
pmc: PMC10842585
doi:
Types de publication
Journal Article
Langues
eng
Pagination
163-171Informations de copyright
© 2023 the author(s), published by De Gruyter.