A 29-year-old male was brought to the neurology department with a complaint of vomiting for one month. He had known mental retardation, epilepsy, and chronic hypocalcemia. His relatives said that… Click to show full abstract
A 29-year-old male was brought to the neurology department with a complaint of vomiting for one month. He had known mental retardation, epilepsy, and chronic hypocalcemia. His relatives said that the patient was diagnosed with phenylketonuria in childhood. As a result of further radiological examination, cranial MR images were compatible with phenylketonuria (â–ºFigure 1A-F). Although our case is very rare, it is worth reminding that phenylketonuria can be
               
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