Skip to main content
Orphanet Journal of Rare Diseases logoLink to Orphanet Journal of Rare Diseases
. 2026 Feb 19;21:67. doi: 10.1186/s13023-026-04268-8

Correction to: Xanthogranulomatous osteomyelitis of the jaw in a young boy: a case report

Kevin Bloch-Maier 1, Sophie-Myriam Dridi 2, Arek Sulukdjian 3, Anne-Laure Ejeil 4,✉
PMCID: PMC12918376  PMID: 41715128

Correction to: Orphanet Journal of Rare Diseases (2025) 20:488

10.1186/s13023-025-04010-w

Following publication of the original article [1], the authors identified an error in the authors names’ order. The given name and family name were erroneously transposed.

The incorrect author’ names are:

Bloch-Maier Kevin 1,

Dridi Sophie-Myriam 2,

Sulukdjian Arek 3 and

Ejeil Anne-Laure 4*

The correct authors’ names are:

Kevin Bloch-Maier 1,

Sophie-Myriam Dridi 2,

Arek Sulukdjian 3 and

Anne-Laure Ejeil 4*

The author group has been updated above and the original article [1] has been corrected.

Footnotes

Publisher’s note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Reference

  • 1.Bloch-Maier, et al. Xanthogranulomatous osteomyelitis of the jaw in a young boy: a case report. Orphanet J Rare Dis. 2025;20:488 10.1186/s13023-025-04010-w. [DOI] [PMC free article] [PubMed]

Articles from Orphanet Journal of Rare Diseases are provided here courtesy of BMC

RESOURCES