Cargando…
46,XY DSD with Female or Ambiguous External Genitalia at Birth due to Androgen Insensitivity Syndrome, 5α-Reductase-2 Deficiency, or 17β-Hydroxysteroid Dehydrogenase Deficiency: A Review of Quality of Life Outcomes
Disorders of sex development refer to a collection of congenital conditions in which atypical development of chromosomal, gonadal, or anatomic sex occurs. Studies of 46,XY DSD have focused largely on gender identity, gender role, and sexual orientation. Few studies have focused on other domains, suc...
Autores principales: | Wisniewski, Amy B., Mazur, Tom |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2009
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2777017/ https://www.ncbi.nlm.nih.gov/pubmed/19956704 http://dx.doi.org/10.1155/2009/567430 |
Ejemplares similares
-
Clinical and Laboratorial Features That May Differentiate 46,XY DSD due to Partial Androgen Insensitivity and 5α-Reductase Type 2 Deficiency
por: Veiga-Junior, Nélio Neves, et al.
Publicado: (2012) -
MON-066 17B-hydroxysteroid dehydrogenase Type 3 Deficiency: An Under-Recognized Cause of 46,XY DSD in the United States?
por: Whitehead, J, et al.
Publicado: (2020) -
“Congruency the ART of Being Real” - 46XY DSD Due to 5 α Reductase Deficiency - Challenges in Decision Making
por: Subbiah, Sridhar, et al.
Publicado: (2021) -
5‐Alpha reductase deficiency; an important cause of 46, XY DSD: Report of three cases within a family
por: Noroozi Asl, Samaneh, et al.
Publicado: (2023) -
What Term to Choose: Ambiguous Genitalia or Disorders of Sex Development (DSD)?
por: Acimi, Smail
Publicado: (2019)