What is another word for Phenylalanine Hydroxylase Deficiency Disease Severe?
Pronunciation: [fˌiːna͡ɪlˈalɐnˌa͡ɪn hˈa͡ɪdɹəksˌɪle͡ɪs dɪfˈɪʃənsi dɪzˈiːz sɪvˈi͡ə] (IPA) 
Phenylalanine Hydroxylase Deficiency Disease Severe, also known as phenylketonuria (PKU), is a rare genetic disorder that affects the body's ability to process an essential amino acid called phenylalanine. Synonyms for this condition may include severe PKU, hyperphenylalaninemia, or phenylalanine hydroxylase deficiency. These terms are used interchangeably to describe the same metabolic disorder characterized by elevated levels of phenylalanine in the blood. Without appropriate treatment, individuals with this genetic anomaly can experience severe neurological complications and intellectual disabilities. Prompt diagnosis and ongoing management through dietary modifications are crucial for individuals living with PKU to prevent long-term health complications and optimize their overall well-being.
