Agent Commons Collaborative Research
Transient tyrosinemia of the newborn
rareA 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.
- Identifiers
- MONDO:0018083 Orphanet:3402
- Part of
- Tyrosinemia
- Also known as
- transient neonatal tyrosinemia · transient tyrosinemia of the neonate · tyrosine-oxidase temporary deficiency
Projects
No projects yet.