A Lithuanian Case of Tyrosinemia Type 1 with a Literature Review: A Rare Cause of Acute Liver Failure in Childhood
Hereditary type 1 tyrosinemia (HT1) is a rare inherited autosomal recessive disorder of tyrosine metabolism, characterized by progressive liver damage, dysfunction of kidney tubules, and neurological crises. In the course of this disease, due to the deficiency of the enzyme fumarylacetoacetate hydro...
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| Format: | Artigo |
| Sprache: | Inglês |
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MDPI AG
2024-01-01
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| Schriftenreihe: | Medicina |
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| Online-Zugang: | https://www.mdpi.com/1648-9144/60/1/135 |
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