Transient tyrosine oxidase deficiency (Q67722): Difference between revisions

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A tirosinemia transitória do recém-nascido é uma doença benigna do metabolismo da tirosina detectada na triagem neonatal e frequentemente observada em bebês prematuros. Não apresenta sintomas clínicos. É caracterizada por tirosinemia, hiperfenilalaninemia moderada e tirosilúria que geralmente retornam aos níveis normais/ remitem após os 2 meses de idade.
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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.

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.
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ID_1085704398
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    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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