phenylketonuria oor Albanees

phenylketonuria

/fɛnʌɪlkiːtəˈnjʊəɹɪə/ naamwoord
en
(medicine) a metabolic disorder in which individuals lack the liver enzyme phenylalanine hydroxylase ( PAH ) which is needed to metabolize the amino acid phenylalanine

Vertalings in die woordeboek Engels - Albanees

Fenilketonuria

en
amino acid metabolic disorder that is characterized by a mutation in the gene for the hepatic enzyme phenylalanine hydroxylase (PAH), rendering it nonfunctional
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Two examples are diabetes mellitus (a multifactorial disorder) and phenylketonuria (an inborn error of metabolism).
Dy shembuj janë diabeti mellitus (një çrregullim multifaktorial) dhe fenilketonuria (një gabim i lindur i metabolizmit).WikiMatrix WikiMatrix
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