Cystinosis: Revision history

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22 March 2026

19 March 2026

  • curprev 14:2314:23, 19 March 2026‎ Danbot talk 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 March 2026

  • curprev 23:4623:46, 17 March 2026‎ Ostermayer talk 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..."
Retrieved from "https://www.wikem.org/wiki/Cystinosis"