A Case of 46 XX Male Syndrome / 대한내분비학회지
Journal of Korean Society of Endocrinology
; : 148-152, 2001.
Artigo
em Coreano
| WPRIM (Pacífico Ocidental)
| ID: wpr-53084
Biblioteca responsável:
WPRO
ABSTRACT
The 46, XX male syndrome is rare disease that is characterized by a phenotypic male who has a 46, XX female karyotype. Since the first report by de la Chapelle and associates in 1964, several cases have been reported, but it is still a rare entity. Recently we examined a 20-year-old XX male who had the symptoms of gynecomastia, an infantile appearance of the external genitalia, scanty pubic hair, no Adams apple, and no axillary hair. We presently describe a patient with the 46, XX male syndrome who showed a 46, XX karyotype on chromosomal study and review the literatures.
Texto completo:
Disponível
Base de dados:
WPRIM (Pacífico Ocidental)
Assunto principal:
Doenças Raras
/
Transtornos Testiculares 46, XX do Desenvolvimento Sexual
/
Cariótipo
/
Genitália
/
Ginecomastia
/
Cabelo
Limite:
Feminino
/
Humanos
/
Masculino
Idioma:
Coreano
Revista:
Journal of Korean Society of Endocrinology
Ano de publicação:
2001
Tipo de documento:
Artigo