Transient tyrosinemia of the newborn
MONDO:0018083A benign disorder of tyrosine metabolism detected upon newborn screening and often observed in premature infants. It shows no clinical symptoms. It is characterized by tyrosinemia, moderate hyperphenylalaninemia, and tyrosiluria that usually resolve after 2 months of age.
Also known as: transient neonatal tyrosinemia, transient tyrosinemia of the neonate, tyrosine-oxidase temporary deficiency
0 clinical trials for this condition and its sub-types.
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Disease
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Metabolic disease
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Hereditary disease
(176)
Inborn errors of metabolism
(45)
Human disease
(14)
Tyrosinemia
(6)
Inborn disorder of amino acid metabolism
(4)
Disease of genetic or genomic mechanism
(2)
Amino acid metabolism disease
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Disease by developmental or physiological process
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