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Nikishina, Irina P; Arsenyeva, Svetlana V; Matkava, Valeria G; Arefieva, Alia N; Kaleda, Mariya I; Smirnov, Alexandr V; Blank, Leonid M; Kostik, Mikhail M
Pediatric rheumatology online journal, 08/2023, Letnik: 21, Številka: 1Journal Article
Fibrodysplasia ossificans progressive (FOP) is an ultra-rare genetic disorder that is caused by a mutation in the ACVR1 gene and provokes severe heterotopic ossification. Since flares of the disease are associated with inflammation, it is assumed that JAK inhibitors can control active FOP due to blocking multiple signaling pathways. Keywords: Fibrodysplasia ossificans progressiva, FOP, Heterotopic ossification, Tofacitinib, Autoinflammation, Spondyloarthritis-like disease, ACVR1 gene, Bone morphogenetic protein, BMP
