Transient tyrosinemia of the newborn

MONDO:0018083

A 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

24 clinical trials for this condition and its sub-types.

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