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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.
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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  Data: Recurrent hemophagocytic lymphohistiocytosis in COG deficiency: a case series and systematic review of inflammatory manifestations.
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  Data: <searchLink fieldCode="AU" term="%22de+Laitre+A%22">de Laitre A</searchLink>; Pediatrics Department CHRU de Tours, Tours, France.<br /><searchLink fieldCode="AU" term="%22Barth+M%22">Barth M</searchLink>; 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.<br /><searchLink fieldCode="AU" term="%22Labarthe+F%22">Labarthe F</searchLink>; 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.<br /><searchLink fieldCode="AU" term="%22Tardieu+M%22">Tardieu M</searchLink>; Pediatrics Department CHRU de Tours, Tours, France; Reference Center for Inborn Errors of Metabolism ToTeM, Tours, France.<br /><searchLink fieldCode="AU" term="%22Lejeune+J%22">Lejeune J</searchLink>; Inserm U1069 N2C, Université de Tours, Tours, France; Service d'Hématologie et d'Oncologie pédiatrique, CHRU de Tours, Tours, France.<br /><searchLink fieldCode="AU" term="%22Goetz+V%22">Goetz V</searchLink>; Pediatrics Department CHRU de Tours, Tours, France; Reference Center for Inborn Errors of Metabolism ToTeM, Tours, France. Electronic address: v.goetz@chu-tours.fr.
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  Data: <searchLink fieldCode="JN" term="%229805456%22">Molecular genetics and metabolism</searchLink> [Mol Genet Metab] 2026 Aug; Vol. 148 (4), pp. 110184. <i>Date of Electronic Publication: </i>2026 Jun 07.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Academic+Press%22">Academic Press </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>9805456 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1096-7206 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2210967192%22">10967192 </searchLink><i>NLM ISO Abbreviation: </i>Mol Genet Metab <i>Subsets: </i>MEDLINE
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        Value: 10.1016/j.ymgme.2026.110184
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      – TitleFull: Recurrent hemophagocytic lymphohistiocytosis in COG deficiency: a case series and systematic review of inflammatory manifestations.
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              Text: 2026 Aug
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