Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Comment
. 2021 Mar 17;19(1):32.
doi: 10.1186/s12969-021-00533-1.

Genetics of chronic nonbacterial osteomyelitis in the irish population: no significant association with rare FBLIM1 variants

Daire O'Leary  1   2 , Orla G Killeen  3 , Anthony G Wilson  4
Affiliations
Comment

Genetics of chronic nonbacterial osteomyelitis in the irish population: no significant association with rare FBLIM1 variants

Daire O'Leary et al. Pediatr Rheumatol Online J. .
No abstract available

Keywords: Autoinflammation; CNO; CRMO; Chronic nonbacterial osteomyelitis; Chronic recurrent multifocal osteomyelitis; FBLIM1 gene.

PubMed Disclaimer

Conflict of interest statement

The authors declare that they have no competing interests.

Comment on

References

    1. d’Adamo AP, Bianco AM, Ferrara G, La Bianca M, Insalaco A, Tommasini A, et al. High prevalence of rare FBLIM1 gene variants in an Italian cohort of patients with Chronic Non-bacterial Osteomyelitis (CNO). Pediatr Rheumatol Online J. 2020 Jul 10;18(1):55. - PMC - PubMed
    1. Cox AJ, Darbro BW, Laxer RM, Velez G, Bing X, Finer AL, et al. Recessive coding and regulatory mutations in FBLIM1 underlie the pathogenesis of chronic recurrent multifocal osteomyelitis (CRMO) PLoS One. 2017;12(3):e0169687. doi: 10.1371/journal.pone.0169687. - DOI - PMC - PubMed
    1. Girschick H, Finetti M, Orlando F, Schalm S, Insalaco A, Ganser G, et al. The multifaceted presentation of chronic recurrent multifocal osteomyelitis: A series of 486 cases from the Eurofever international registry. Rheumatol (United Kingdom). 2018;57(7). - PubMed
    1. Assmann G, Köhm M, Schuster V, Behrens F, Mössner R, Magnolo N, et al. Genetic variants in FBLIM1 gene do not contribute to SAPHO syndrome and chronic recurrent multifocal osteomyelitis in typical patient groups. BMC Med Genet. 2020 Dec 12;21(1):102. - PMC - PubMed
    1. Roderick MR, Ramanan AV. Chronic recurrent multifocal osteomyelitis. Adv Exp Med Biol. 2013;764:99–107. doi: 10.1007/978-1-4614-4726-9_7. - DOI - PubMed

LinkOut - more resources