hydroxyphenyluria
hy·drox·y·phen·yl·u·ri·a
(hī-drok'sē-fen'il-yū'rē-ă),Urinary excretion of tyrosine and phenylalanine, as a result of ascorbic acid deficiency; occurs notably in those premature infants who lack this vitamin.
Farlex Partner Medical Dictionary © Farlex 2012
hy·drox·y·phen·yl·u·ri·a
(hī-drok'sē-fen'il-yūr'ē-ă)Urinary excretion of tyrosine and phenylalanine, as a result of ascorbic acid deficiency; occurs notably in those premature infants who lack this vitamin.
Medical Dictionary for the Health Professions and Nursing © Farlex 2012