A Case of 46 XX Male Syndrome / 대한내분비학회지
Journal of Korean Society of Endocrinology
;
: 148-152, 2001.
Article
in Korean
| WPRIM
| ID: wpr-53084
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.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Rare Diseases
/
46, XX Testicular Disorders of Sex Development
/
Karyotype
/
Genitalia
/
Gynecomastia
/
Hair
Limits:
Female
/
Humans
/
Male
Language:
Korean
Journal:
Journal of Korean Society of Endocrinology
Year:
2001
Type:
Article
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