Historial de revisiones de «Cystinosis»

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22 mar 2026

19 mar 2026

  • actant 14:2314:23 19 mar 2026‎ Danbot discusión contribs.‎ 11 932 bytes −248‎ Moved intro paragraph into Background as bullets; removed excessive bold from bullet lead-ins; added Renal tubular disorders DDX template; bold retained for critical items only

17 mar 2026

  • actant 23:4623:46 17 mar 2026‎ Ostermayer discusión contribs.‎ 12 172 bytes +12 172‎ Created page with "Cystinosis is a rare autosomal recessive lysosomal storage disorder caused by mutations in the '''CTNS''' gene, resulting in accumulation of the amino acid cystine within lysosomes of all cells. It is the '''most common inherited cause of Fanconi syndrome''' in children.<ref name="StatPearls">Cystinosis. ''StatPearls''. 2024. PMID: 39548762</ref> Emergency physicians encounter cystinosis patients presenting with '''severe dehydration''', '''electrolyte crises''' (hyp..."
Obtenido de «https://www.wikem.org/wiki/Cystinosis»