Transient tyrosine oxidase deficiency (Q67722): Difference between revisions
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Latest 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 |
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| 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. |
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CID11:ID_1085704398
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dki-india-ID_1085704398
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Concluído
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13 August 2026
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