Tyrosinemia: Revision history

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22 March 2026

19 March 2026

17 March 2026

  • curprev 23:5123:51, 17 March 2026‎ Ostermayer talk contribs‎ 12,342 bytes +12,342‎ Created page with "Tyrosinemia refers to a group of inherited disorders of tyrosine metabolism. '''Tyrosinemia type 1 (HT1)''' is the most severe and EM-relevant form, caused by deficiency of fumarylacetoacetate hydrolase (FAH), leading to accumulation of toxic metabolites that cause '''acute liver failure''', '''Fanconi syndrome''', '''porphyria-like neurologic crises''', and '''hepatocellular carcinoma'''.<ref name="GeneReviews">Tyrosinemia Type I. ''GeneRevie..."
Retrieved from "https://www.wikem.org/wiki/Tyrosinemia"