Cargando…
Review of Outcome Information in 46,XX Patients with Congenital Adrenal Hyperplasia Assigned/Reared Male: What Does It Say about Gender Assignment?
There is ample historical verification of 46,XX congenital adrenal hyperplasia (CAH) patients being born with essentially male genitaliawhile outcome information is scant. Prior to glucocorticoid therapy, most patients died very young from adrenal insufficiency. Most available reports from laterchil...
Autores principales: | Lee, Peter A., Houk, Christopher P. |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3010645/ https://www.ncbi.nlm.nih.gov/pubmed/21197442 http://dx.doi.org/10.1155/2010/982025 |
Ejemplares similares
-
Gender of rearing and psychosocial aspect in 46 XX congenital adrenal hyperplasia
por: Gangaher, Arushi, et al.
Publicado: (2016) -
Male genitoplasty for 46 XX congenital adrenal hyperplasia patients presenting late and reared as males
por: Sharma, Shilpa, et al.
Publicado: (2012) -
Fully Masculinized 46,XX Individuals with Congenital Adrenal
Hyperplasia: Perspective Regarding Sex of Rearing and Surgery
por: L Jones, Collin, et al.
Publicado: (2022) -
Clinical Characteristics of 46,XX Males with Congenital Adrenal Hyperplasia
por: Savaş-Erdeve, Şenay, et al.
Publicado: (2021) -
Male Gender Identity and Reversible Hypokalemic Hypertension in a 46,XX Child with 11-Beta-Hydroxylase Deficiency Congenital Adrenal Hyperplasia
por: Goyal, Alpesh, et al.
Publicado: (2019)