Searchable abstracts of presentations at key conferences in endocrinology

ea0081ep837 | Pituitary and Neuroendocrinology | ECE2022

Kallmann’s Syndrome: case report

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...

ea0070aep556 | General Endocrinology | ECE2020

Autoimmune polyglandular syndrome (APS) type 2 associated with chronic kidney disease

El Ebrashy Ibrahim , ElHaddad Hemmat , Moustafa Heba , El Rawi Hoda , Amin Samar , Taraby Aya , Salam Randa , Magdi Mohamed

Introduction: Autoimmune polyglandular syndrome (APS) is a rare disease, that is defined by the presence of two or more glandular insufficiencies caused by autoimmune mechanisms and that may be associated with other pathologies and immunological phenomena. It is characterized by the Presence of circulating organ specific antibodies and lymphocytic infiltration of the affected gland.Case report: A 38-year-old female known to have autoimmune polyglandular ...