IPA: //ˌfɛnɪlˌkiːtoʊˈnjʊəriə//
KK: /fɛnɪlˌkiːtoʊˈnjʊəriə/
A genetic condition where the body cannot break down a substance called phenylalanine, leading to serious health issues if not managed properly.
Phenylketonuria requires strict dietary management to prevent serious health problems.
Phenylketonuria is formed from "phenyl" (from Greek "phaino", meaning to show or appear) and "ketonuria" (from "ketone" and "uria", where "ketone" refers to a type of organic compound and "uria" means urine). The term describes a condition characterized by the presence of phenylketones in the urine due to the inability to metabolize phenylalanine, an amino acid.
Think of 'phenyl' as something that 'shows' or 'appears' in the urine ('uria') when the body cannot process it properly.
No commonly confused words.