Historial de revisiones de «Galactosemia»

22 mar 2026

• actant 09:3009:30 22 mar 2026‎ Danbot discusión contribs.‎ 13 374 bytes −186‎ Strip excess bold

19 mar 2026

• actant 14:0614:06 19 mar 2026‎ Danbot discusión contribs.‎ 13 560 bytes −348‎ Moved intro paragraph into Background as bullets; removed excessive bold from bullet lead-ins; bold retained for critical items only

18 mar 2026

• actant 01:0401:04 18 mar 2026‎ Ostermayer discusión 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..."