MALE PSEUDOHERMAPHRODITISM WITH 5-ALPHA-REDUCTASE DEFICIENCY - REPORTOF 2 NEW FAMILIAL CASES - THE IMPORTANCE OF EARLY DIAGNOSIS

Citation
M. Aguilardiosdado et al., MALE PSEUDOHERMAPHRODITISM WITH 5-ALPHA-REDUCTASE DEFICIENCY - REPORTOF 2 NEW FAMILIAL CASES - THE IMPORTANCE OF EARLY DIAGNOSIS, Journal of pediatric endocrinology & metabolism, 8(1), 1995, pp. 67-71
Citations number
14
Categorie Soggetti
Pediatrics,"Endocrynology & Metabolism
ISSN journal
0334018X
Volume
8
Issue
1
Year of publication
1995
Pages
67 - 71
Database
ISI
SICI code
0334-018X(1995)8:1<67:MPW5D->2.0.ZU;2-H
Abstract
We report two new familial cases of male pseudohermaphroditism due to 5-alpha-reductase deficiency, from the south of Spain. They were born with ambiguous genitalia and were reared as females. At the time of pu berty, both brothers virilized partially and underwent a change of gen der role from female to male with a stormy psychic readjustment period . We stress the value of the prolonged chorionic gonadotropin test for an early diagnosis.