Causes, Symptoms, Intellectual Disability, Behavioural Issues, Skin Conditions, Microcephaly, Seizures, Management, Regular Monitoring, Nutrition a Supplementation, Support As Well As Counselling of Classical PKD and Symptoms, Treatment As Well As Managem

Abstract

Phenylketonuria (PKU) is a genetic disorder with an incidence of approximately 1 in 10,000 to 15,000 births worldwide. Phenylketonuria is an inherited metabolic disorder manifested by the lack  of  ability to metabolize phenylalanine, an amino acid found in many protein-rich foods. This review provides a detailed overview of PKU, including its types, clinical manifestations, and management strategies. The understanding of PKU has developed  over the years, leading to improved diagnosis and treatment approaches. Early detection and intervention play a crucial role in obstructing  intellectual disabilities and ensuring a better quality of life for individuals with PKU.