Copyright: ©Author(s) 2026.
World J Clin Pediatr. Sep 9, 2026; 15(3): 120925
Published online Sep 9, 2026. doi: 10.5409/wjcp.120925
Published online Sep 9, 2026. doi: 10.5409/wjcp.120925
Table 1 Clinical timeline: Episodes of acute liver failure
| Age | Trigger | Key laboratory findings | Treatment | Outcome |
| 19 months | Fever + URTI; antibiotics and paracetamol given | ALT: 1840, AST: 2210, Bili: 340 μmol/L, GGT: 18 (low), INR: 2.8, pancytopenia | Corticosteroids, IV fluids, nutritional support | Partial improvement; no normalisation |
| 21 months | Febrile illness | ALT: 980, AST: 1140, Bili: 210, GGT: 20, INR: 2.1 | Supportive care; steroids repeated | Partial improvement; ongoing enzyme elevation |
| 22 months | Febrile UTI | ALT: 2100, AST: 2450, Bili: 380 μmol/L, INR: 3.1, GGT: 24, Plt: 62 | Antibiotics + supportive care | Ongoing follow-up; genetic counselling initiated |
- Citation: Zourob D, Teneiji AA, Miqdady M, Al Atrash E. Recurrent acute liver failure in infancy - a novel SCYL1 mutation: A case report. World J Clin Pediatr 2026; 15(3): 120925
- URL: https://www.wjgnet.com/2219-2808/full/v15/i3/120925.htm
- DOI: https://dx.doi.org/10.5409/wjcp.120925