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.

Keyword

Kallmann syndrome; Hypogonadotropic hypogonadism; Anosmia

MeSH Terms

Brain
Gonadotropin-Releasing Hormone
Hypogonadism
Kallmann Syndrome*
Magnetic Resonance Imaging
Olfaction Disorders
Gonadotropin-Releasing Hormone
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