Male pseudohermaphroditism due to partial end-organ insensitivity to androgens.
Clin Endocrinol (Oxf)
; 7(2): 137-41, 1977 Aug.
Article
em En
| MEDLINE
| ID: mdl-890997
ABSTRACT
A 46XY individual with incomplete male pseudohermaphroditism was studied. The phenotype was distinctive, with a masculine habitus despite a small phallus, gynaecomastia and diminished virilization. Plasma levels of testosterone, oestrogens, gonadotrophins and sex-hormone binding globulin were elevated. It is proposed that this syndrome is a variant of Type I incomplete male pseudohermaphroditism.
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Bases de dados:
MEDLINE
Assunto principal:
Transtornos do Desenvolvimento Sexual
/
Receptores Androgênicos
/
Receptores de Esteroides
Limite:
Adult
/
Humans
/
Male
Idioma:
En
Revista:
Clin Endocrinol (Oxf)
Ano de publicação:
1977
Tipo de documento:
Article