TY - CHAP M1 - Book, Section TI - Kallmann Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e 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). SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/29 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164074617 ER -