Two Cases of Kallmann Syndrome / 대한소아내분비학회지
Journal of Korean Society of Pediatric Endocrinology
;
: 179-183, 2003.
Article
in Korean
| WPRIM
| ID: wpr-138139
ABSTRACT
Kallmann syndrome is characterized by hypogonadotropic hypogonadism resulting from insufficient release of GnRH and associated with anosmia or hyposmia. We experienced two cases of Kallmann syndrome with abnormal brain MRI findings(olfactory bulb aplasia) & secondary sexual dysfunction.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Brain
/
Magnetic Resonance Imaging
/
Gonadotropin-Releasing Hormone
/
Kallmann Syndrome
/
Hypogonadism
/
Olfaction Disorders
Language:
Korean
Journal:
Journal of Korean Society of Pediatric Endocrinology
Year:
2003
Type:
Article
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