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Kallmann syndrome is a rare inherited disorder characterized by hypogonadotropic hypogonadism and anosmia or hyposmia. Such cases are mostly diagnosed in adolescent period with complaints of failure to achieve puberty. Early diagnosis and treatment can restore secondary sexual characteristics in such patients. We report a case of a 17-year-old male with Kallmann syndrome who came with hypogonadism and bimanual synkinesis.