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What is another word for Atypical Phenylketonuria?

Pronunciation: [e͡ɪtˈɪpɪkə͡l fˌiːna͡ɪlkˌɛtənjˈʊɹi͡ə] (IPA)

Atypical Phenylketonuria, often abbreviated as PKU, is a rare genetic disorder characterized by the inability to properly metabolize an essential amino acid called phenylalanine. This disorder can lead to an accumulation of this amino acid in the body, causing a variety of symptoms such as intellectual disability, behavioral problems, and seizures. However, while "Atypical Phenylketonuria" is the specific term used to describe this condition, there are a few alternative synonyms that can be used interchangeably. These include Non-classic Phenylketonuria, Variant Phenylketonuria, and Atypical PKU. Despite the different names, they all refer to the same metabolic disorder affecting the body's ability to process phenylalanine.
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What are the opposite words for Atypical Phenylketonuria?

Atypical Phenylketonuria is a rare metabolic disorder that affects the body's ability to process the amino acid phenylalanine. Antonyms for Atypical Phenylketonuria would be typical, normal or common. Most individuals are born with the ability to break down phenylalanine properly. However, in cases of Phenylketonuria, the body fails to produce the enzyme necessary to metabolize phenylalanine. This results in a buildup of the amino acid, which can be toxic to the brain and cause developmental delays. A typical Phenylketonuria diagnosis usually occurs during newborn screening, allowing for prompt treatment through dietary modifications. In contrast, Atypical Phenylketonuria may present with milder symptoms or later in life, making diagnosis and treatment more challenging.

What are the antonyms for Atypical phenylketonuria?

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