Transient tyrosine oxidase deficiency (Q67722)
From determinar.ia.br - Determine suas informações
Transient tyrosinemia of the newborn is a benign disorder of tyrosine metabolism detected upon newborn screening and often observed in premature infants. It shows no clinical symptoms. It is characterised by tyrosinemia, moderate hyperphenylalaninemia, and tyrosiluria that usually resolve after 2 months of age.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1085704398 |
||
| English | Transient tyrosine oxidase deficiency |
Transient tyrosinemia of the newborn is a benign disorder of tyrosine metabolism detected upon newborn screening and often observed in premature infants. It shows no clinical symptoms. It is characterised by tyrosinemia, moderate hyperphenylalaninemia, and tyrosiluria that usually resolve after 2 months of age. |
Statements
CID11:ID_1085704398
0 references
dki-india-ID_1085704398
0 references
Concluído
0 references
13 August 2026
0 references
