How Do You Spell CLASSICAL PHENYLKETONURIAS?

Pronunciation: [klˈasɪkə͡l fˌiːna͡ɪlkˌɛtənjˈʊɹi͡əz] (IPA)

Classical Phenylketonurias refers to a group of genetic disorders that affect the body's ability to process the amino acid phenylalanine. The IPA phonetic transcription for this word is /klæsɪkəl fi:nɪlkitoʊ'njʊriəz/. It is important to note that the "ph" in "phenylketonurias" is pronounced with an "f" sound (/fi:nɪl/), not a "p" sound. Classical Phenylketonurias can be treated through a low-phenylalanine diet and early detection through newborn screening can greatly improve outcomes.

CLASSICAL PHENYLKETONURIAS Meaning and Definition

1. Classical phenylketonurias (PKU) is a term used to describe a group of inherited metabolic disorders that affect the body's ability to break down an amino acid called phenylalanine. This condition is caused by a deficiency or absence of an enzyme called phenylalanine hydroxylase (PAH).

   Phenylalanine is obtained through the diet from certain protein-containing foods, and normally, the enzyme PAH converts phenylalanine into another amino acid called tyrosine. However, in classical PKU, the lack of PAH activity leads to the accumulation of phenylalanine in the blood and body tissues, which can lead to various neurological and developmental problems.

   The symptoms of classical PKU typically become apparent within a few months after birth. Without treatment, affected individuals may develop intellectual disability, developmental delay, seizures, behavioral issues, and issues with executive functioning. However, when diagnosed early and treated with a controlled diet low in phenylalanine, individuals with classical PKU can lead normal lives and prevent or minimize the associated complications.

   Genetic mutations in the PAH gene are responsible for classical PKU, and the condition follows an autosomal recessive inheritance pattern, meaning that both copies of the gene must be affected to develop the condition.

   Overall, classical phenylketonurias is a group of genetic disorders characterized by the inability to properly metabolize phenylalanine due to a deficiency or absence of the enzyme phenylalanine hydroxylase. Early diagnosis and a lifelong restricted diet can help individuals with this condition lead normal lives and prevent cognitive and neurological complications.

Common Misspellings for CLASSICAL PHENYLKETONURIAS

• xlassical phenylketonurias
• vlassical phenylketonurias
• flassical phenylketonurias
• dlassical phenylketonurias
• ckassical phenylketonurias
• cpassical phenylketonurias
• coassical phenylketonurias
• clzssical phenylketonurias
• clsssical phenylketonurias
• clwssical phenylketonurias
• clqssical phenylketonurias
• claasical phenylketonurias
• clazsical phenylketonurias
• claxsical phenylketonurias
• cladsical phenylketonurias
• claesical phenylketonurias
• clawsical phenylketonurias
• clasaical phenylketonurias
• claszical phenylketonurias
• clasxical phenylketonurias

Etymology of CLASSICAL PHENYLKETONURIAS

The term "Classical Phenylketonurias" is derived from two main components:

1. Classical: The word "classical" is an adjective that refers to something traditional, well-established, or typical. In this context, it implies the most common and well-known form of phenylketonurias.

2. Phenylketonurias: The term "phenylketonurias" is a plural noun that refers to a group of inherited metabolic disorders. It is composed of two main components:

- Phenylketonuria: The word "phenylketonuria" is a compound noun that combines "phenyl", derived from the aromatic compound called "phenylalanine", and "ketonuria", which refers to the presence of ketones in the urine.