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

• मुख्य लेखकों: Gunter Assmann (लेखक), Michaela Köhm (लेखक), Volker Schuster (लेखक), Frank Behrens (लेखक), Rotraut Mössner (लेखक), Nina Magnolo (लेखक), Vinzenz Oji (लेखक), Harald Burkhardt (लेखक), Ulrike Hüffmeier (लेखक)
• स्वरूप: पुस्तक
• प्रकाशित: BMC, 2020-05-01T00:00:00Z.
• विषय: article
• ऑनलाइन पहुंच: 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...