Recurrent hemophagocytic lymphohistiocytosis in COG deficiency: a case series and systematic review of inflammatory manifestations.
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| Title: | Recurrent hemophagocytic lymphohistiocytosis in COG deficiency: a case series and systematic review of inflammatory manifestations. |
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| Authors: | de Laitre A; Pediatrics Department CHRU de Tours, Tours, France., Barth M; Genetics Department, Angers Hospital, F-49000 Angers, France; Univ Angers, [CHU Angers], Inserm, CNRS, MITOVASC, Équipe CARME ou Equipe MITOLAB, SFR ICAT, F-49000 Angers, France., Labarthe F; Pediatrics Department CHRU de Tours, Tours, France; Reference Center for Inborn Errors of Metabolism ToTeM, Tours, France; Inserm U1069 N2C, Université de Tours, Tours, France., Tardieu M; Pediatrics Department CHRU de Tours, Tours, France; Reference Center for Inborn Errors of Metabolism ToTeM, Tours, France., Lejeune J; Inserm U1069 N2C, Université de Tours, Tours, France; Service d'Hématologie et d'Oncologie pédiatrique, CHRU de Tours, Tours, France., Goetz V; Pediatrics Department CHRU de Tours, Tours, France; Reference Center for Inborn Errors of Metabolism ToTeM, Tours, France. Electronic address: v.goetz@chu-tours.fr. |
| Source: | Molecular genetics and metabolism [Mol Genet Metab] 2026 Aug; Vol. 148 (4), pp. 110184. Date of Electronic Publication: 2026 Jun 07. |
| Publication Type: | Journal Article; Systematic Review; Case Reports; Review |
| Journal Info: | Publisher: Academic Press Country of Publication: United States NLM ID: 9805456 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1096-7206 (Electronic) Linking ISSN: 10967192 NLM ISO Abbreviation: Mol Genet Metab Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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