phe·nyl·ke·ton·uria /ˌfɛnḷˌkitṇˈʊriə, ˌfi, ˈjʊr-/
苯丙酮尿; 苯丙酮酸尿
phe·nyl·ke·ton·uria /ˌfɛnḷˌkɪtṇˈ(j)ʊrɪə, ˌfɪn-/ 名詞
苯丙酮酸尿,苯丙酮尿症
phenylketonuria
n : a genetic disorder of metabolism; lack of the enzyme needed
to turn phenylalanine into tyrosine results in an
accumulation of phenylalanine in the body fluids which
causes various degrees of mental deficiency [syn: PKU]