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What is another word for Phenylalanine Hydroxylase Deficiency Disease?

Pronunciation: [fˌiːna͡ɪlˈalɐnˌa͡ɪn hˈa͡ɪdɹəksˌɪle͡ɪs dɪfˈɪʃənsi dɪzˈiːz] (IPA)

Phenylalanine Hydroxylase Deficiency Disease, also known as phenylketonuria (PKU), is a rare genetic disorder that affects the body's ability to break down an amino acid called phenylalanine. Individuals with PKU must follow a strict low-phenylalanine diet to prevent the accumulation of this amino acid, which can lead to severe brain damage and intellectual disabilities. Although PKU is the most commonly used synonym for Phenylalanine Hydroxylase Deficiency Disease, other terms include phenylketonuria metabolic disorder, phenylalanine hydroxylase deficiency syndrome, or PAH deficiency. Regardless of the terminology used, early diagnosis and management are crucial in ensuring a healthy life for those living with this condition.
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What are the opposite words for Phenylalanine Hydroxylase Deficiency Disease?

Phenylalanine Hydroxylase Deficiency Disease is a rare genetic disorder that affects the body's ability to metabolize the amino acid phenylalanine, leading to a buildup of toxic levels in the body. While there are no direct antonyms for this precise term, antonyms related to the symptoms and complications of the disease could be normal metabolism, absence of toxic buildup, and adequate levels of phenylalanine in the body. Early detection, strict adherence to low-phenylalanine diets, and supplementing with certain amino acids can help prevent complications such as intellectual disability, seizures, and behavioral problems.

What are the antonyms for Phenylalanine hydroxylase deficiency disease?

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