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Ann Pediatr Endocrinol Metab > Volume 8(2); 2003 > Article
Two Cases of Kallmann Syndrome.
Hye Jung Han, Hee Jin Cho, Hye Sun Lee, In Sil Lee, Il Tae Hwang
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.
Keywords: Kallmann syndrome;Hypogonadotropic hypogonadism;Anosmia


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