Maja Đorđević

Associate professor Maja Đorđević Milošević,

Mother and Child Health care Institute of Serbia

She is the head of the department which is the only one in Serbia specializing in Inbor Errors of Metabolism (IEM). She completed her doctoral studies at the Department of Medical Genetics at the University of Belgrade’s Medical Faculty, with a thesis on the genotype-phenotype correlation of patients with phenylketonuria. She teaches inherited metabolic diseases at the subspecialty Department of Medical Genetics. She is involved in organization of the neonatal screening. She has participated in publishing several papers in the field of metabolic diseases. She was the editor of a postgraduate textbook in Pediatrics for ten years. In addition to diagnosing and managing patients from various groups of IEM, due to the large number of patients in Serbia, she has extensive experience in the diagnosis and treatment of patients with glycogen storage disease type 1. She is a member of the national Commissions for Rare Diseases responsible for organizing the diagnosis and treatment of patients with Inborn Errors of Metabolism (IEM). She is a member of SSIEM.