Transient tyrosine oxidase deficiency (Q67722): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / Knowledge Architect | |||
| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||
Normal rank | |||
Revision as of 15:33, 14 August 2026
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
