ea0081ep837 | Pituitary and Neuroendocrinology | ECE2022
Aziz Rokya Abdel
, Moustafa Heba
, Sultan Soad
, Salam Randa
, Garhi Ola El
, Tohamy Iman
, Taraby Aya
, Nashat Amira
Introduction: Kallmann syndrome, a rare genetic disorder, refers to the association between hypogonadotropic hypogonadism and anosmia or hyposmia due to abnormal migration of olfactory axons and gonadotropin-releasing hormone producing neurons It can be autosomal dominant, autosomal recessive, or X-linked inheritance.Case report: A 16-year-old male student, presented to endocrinology unit with delayed puberty. He was born to consanguineous parents and ha...