J Korean Soc Pediatr Endocrinol.
2003 Dec;8(2):179-183.
Two Cases of Kallmann Syndrome
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.