Abstract |
Steroid 5alpha-reductase deficiency is a rare, male-limited autosomal recessive disorder caused by mutation in the SRD5A2 gene resulting in a deficiency of dihydrotestosterone (DHT) during fetal development. Here we report an affected 46,XY adolescent who was born with incompletely virilized genitalia and was raised in the female gender. At 12 years of age, the patient requested feminizing genital surgery. Surgery was withheld and psychiatric counseling was instituted. At 14 years of age, the patient's gender identity and role appeared to be in transition from a female to an increasingly male gender. This case demonstrates that in patients with disorders such as 5alpha-reductase deficiency, in which significant prenatal androgen exposures are combined with postnatal virilization, adult gender identity and gender role may be a dynamic process that is not complete until well after adolescence.
|
Authors | Christopher P Houk, D Damiani, Peter A Lee |
Journal | Journal of pediatric endocrinology & metabolism : JPEM
(J Pediatr Endocrinol Metab)
Vol. 18
Issue 4
Pg. 339-45
(Apr 2005)
ISSN: 0334-018X [Print] Germany |
PMID | 15844467
(Publication Type: Case Reports, Journal Article, Review)
|
Chemical References |
- 3-Oxo-5-alpha-Steroid 4-Dehydrogenase
|
Topics |
- 3-Oxo-5-alpha-Steroid 4-Dehydrogenase
(deficiency)
- Adolescent
- Adolescent Development
- Gender Identity
- Gonadal Dysgenesis, 46,XY
(enzymology, physiopathology, psychology)
- Humans
- Male
|