Transient tyrosinemia of the newborn

Orpha code: 3402OMIM code:

Definition

A rare disorder of tyrosine metabolism characterized by tyrosinemia, moderate hyperphenylalaninemia, and tyrosiluria that usually resolve after 2 months of age. It shows no clinical symptoms and is detected upon newborn screening. It is often observed in premature infants.

Disease data
Classification

Disease

Synonyms
Transient tyrosinemia of the neonate
Przejściowa tyrozynemia noworodków
ORPHA code
3402
OMIM code
-
ICD10 code
P74.5
ICD11 code
5C50.1Y

No additional description.

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