2019
DOI: 10.1210/js.2019-00082
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Sexuality in Males With Congenital Adrenal Hyperplasia Resulting From 21-Hydroxylase Deficiency

Abstract: Purpose Although sexuality has been reported to be impaired in females with congenital adrenal hyperplasia (CAH) resulting from 21-hydroxylase deficiency, sexuality in males with CAH so far has remained largely unconsidered. Patients One of the largest European male cohorts of patients with CAH in which sexuality in male patients with CAH was assessed. Methods … Show more

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Cited by 9 publications
(8 citation statements)
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References 55 publications
(55 reference statements)
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“…In adult males with CAH sexual satisfaction was in general similar to controls/general population [96,116].…”
Section: Article In Presssupporting
confidence: 55%
See 1 more Smart Citation
“…In adult males with CAH sexual satisfaction was in general similar to controls/general population [96,116].…”
Section: Article In Presssupporting
confidence: 55%
“…Long-term negative effects of genital surgery on genital/clitoral sensitivity can contribute to lower satisfaction with sexual function [ 115 ]. In adult males with CAH sexual satisfaction was in general similar to controls/general population [ 96 , 116 ].…”
Section: Miscellaneousmentioning
confidence: 81%
“…Results of numerous studies of women with CAH show that these women are less likely to be exclusively or almost exclusively heterosexual compared with women who do not have CAH, and some of these studies show a positive association with severity of the disorder (Hines, 2011a). In contrast, most studies in men with CAH find little difference in sexual orientation (Gehrmann et al, 2019). Androgen insensitivity syndrome (AIS) is an intersex condition that results in partial or complete inability of the cell to respond to androgens.…”
Section: Introductionmentioning
confidence: 99%
“…Subtle findings such as hyperpigmentation of the scrotum or an enlarged phallus are frequently missed. 13 Hence males are particularly prone to the occurrence of associated salt adrenal crisis and death. 14 Female infants with classic 21-OHD are typically born with atypical genitalia characterized by clitoral enlargement labial fusion, and formation of a urogenital sinus and rarely, virilization may be so profound that genital atypia is unrecognized, and are assigned as males.…”
Section: Discussionmentioning
confidence: 99%