Galactosemia: Revision history

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22 March 2026

19 March 2026

18 March 2026

  • curprev 01:0401:04, 18 March 2026‎ Ostermayer talk contribs‎ 13,908 bytes +13,908‎ Created page with "Galactosemia is an autosomal recessive disorder of galactose metabolism, most commonly caused by '''deficiency of galactose-1-phosphate uridylyltransferase (GALT)''', resulting in toxic accumulation of '''galactose-1-phosphate''' and '''galactitol''' in the liver, brain, kidneys, and lens.<ref name="GeneReviews">Classic Galactosemia and Clinical Variant Galactosemia. ''GeneReviews''. NCBI. 2021.</ref> Classic galactosemia is a '''neonatal emergency''' — affected infant..."
Retrieved from "https://www.wikem.org/wiki/Galactosemia"