Compulsory medical service for Republic of Turkey.
Practicing as solo physician in Southeastern Anatolia Region, in charge of more than 300 children with wide range of ultra-rare inborn errors of metabolism (Phenlyketonuria, MSUD, Tyrosinemia, Mucopolysaccharidosis, etc.)
Has diagnosed hundreds of new patients with IEM (40 MPS, 20 PKU, 10 MSUD, 20 congenital lactic acidosis, etc.)
Responsible for the National Newborn Screening Program.
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