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Gender Identity and Questioning in Klinefelter's Syndrome

AIMS: KS is a congenital condition with 47, XXY chromosome karyotype. Due to a lack of understanding of the condition amongst healthcare providers, KS is grossly underdiagnosed, with most patients never receiving a diagnosis. Within this population, gender dysphoria is suggested to be of higher inci...

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Detalles Bibliográficos
Autores principales: Cai, Valerie, Yap, Tet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9378311/
http://dx.doi.org/10.1192/bjo.2022.176