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

• Main Authors: Gunter Assmann (Author), Michaela Köhm (Author), Volker Schuster (Author), Frank Behrens (Author), Rotraut Mössner (Author), Nina Magnolo (Author), Vinzenz Oji (Author), Harald Burkhardt (Author), Ulrike Hüffmeier (Author)
• Format: Book
• Published: BMC, 2020-05-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Abstract 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...