ea0070ep310 | Pituitary and Neuroendocrinology | ECE2020
Elamin Yasir
, Hussain Al-Qahtani Mohammad
, Mohammed Alabdrabalnabi Fatimah
, Abdulwahed Al Saeed Zahra
Kallmann syndrome is a rare congenital hypogonadotropic hypogonadism with variable degrees of hyposomia to anosmia. This syndrome can be transmitted as autosomal dominant, autosomal recessive and X-linked inheritance pattern. We are reporting two cases of young male siblings (17 and 16 years old) who are the offspring of unrelated parents, presenting with delayed puberty and both were complaining of hyposmia. Their older brother, aged 24 years, was diagnosed with isolated hypo...