Article

Seropositive rheumatoid arthritis in osteogenesis imperfecta type XI (FKBP10 mutation): First case report and literature review

2025-06-30

Abstract excerpt

<title>Abstract</title> <p> <bold>Background:</bold> Osteogenesis imperfecta (OI) is a rare genetic disorder primarily caused by mutations in genes involved in type I collagen production. We report a 27-year-old female with genetically confirmed OI type XI (OI-XI) who experienced a delayed diagnosis of seropositive rheumatoid arthritis (RA), resulting in irreversible deformities. <bold>Case Presentation:</bold...

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Literature Corpus work: 880bdac1-3973-53cd-8d04-142d8500662f
DOI: 10.21203/rs.3.rs-6950688/v1

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