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Article

Genetic variants in FBLIM1 gene do not contribute to SAPHO syndrome and chronic recurrent multifocal osteomyelitis in typical patient groups.

BMC medical genetics - 12 May 2020

Assmann Gunter, Köhm Michaela, Schuster Volker, Behrens Frank, Mössner Rotraut, Magnolo Nina, Oji Vinzenz, Burkhardt Harald, Hüffmeier Ulrike

Abstract excerpt

BACKGROUND: Syndrome of synovitis acne pustulosis hyperostosis osteitis (SAPHO) and chronic recurrent multifocal osteomyelitis (CRMO) present two diseases of a dermatologic and rheumatologic spectrum that are variable in manifestation und therapeutic response. Genetic risk factors have long been assumed in both diseases, but no single reliable factor has been identified yet. Therefore, we aimed to clinically...

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Identifiers

PMID: 32397996
DOI: 10.1186/s12881-020-01037-7
PMCID: PMC7216525

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