Nutrients, Vol. 18, Pages 146: Cognitive Functioning in Phenylketonuria: A Lifespan Perspective
Nutrients, Vol. 18, Pages 146: Cognitive Functioning in Phenylketonuria: A Lifespan Perspective Nutrients doi: 10.3390/nu18010146 Authors: Stephan Huijbregts Cristina Romani Phenylketonuria (PKU) is a hereditary metabolic disorder characterized by the inability to metabolize phenylalanine, leading to neurotoxic accumulation of phenylalanine and significant cognitive impairment. While extensive research has focused on the cognitive outcomes in middle
