Clinical characteristics of two patients with Tyrosinemia type I in Slovenia

Published: 1 November 2021| Version 1 | DOI: 10.17632/hcyth2z3xv.1
Contributor:
Jaka Šikonja

Description

To support our results we share with the scientific community the data behind the analysis of the only two patients with tyrosinemia type I in Slovenia. The data was obtained from the Electronic Health Records at the University Children's Hospital, University Medical Centre.

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Categories

Succinylacetone, Genetic Disorder, Inborn Error of Metabolism, Metabolism, Liver Disease, Newborn Screening, Phenylalanine, Orphan Disorder, Tyrosine

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