RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164074617 T1 Kallmann Syndrome T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e YR 2019 FD 2019 PB McGraw-Hill Education PP New York, NY SN 9781259861789 LK accesspediatrics.mhmedical.com/content.aspx?aid=1164074617 RD 2024/03/29 AB It is a congenital syndrome characterized by the association of hypogonadotropic hypogonadism with anosmia (or hyposmia). It is characterized by failure of puberty. Left untreated, patients with Kallmann Syndrome will almost invariably be infertile. The condition can occur in both males and females, but is more commonly diagnosed in males (4:1).