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  1. Article

    Open Access

    Scoliosis in osteogenesis imperfecta: identifying the genetic and non-genetic factors affecting severity and progression from longitudinal data of 290 patients

    Scoliosis is widely prevalent among osteogenesis imperfecta (OI) patients, and is progressive with age. However, factors affecting scoliosis in OI are not well known.

    Peikai Chen, Yapeng Zhou, Zhijia Tan, Yunzhi Lin in Orphanet Journal of Rare Diseases (2023)

  2. Article

    Open Access

    Patient-reported outcomes in a Chinese cohort of osteogenesis imperfecta unveil psycho-physical stratifications associated with clinical manifestations

    Osteogenesis imperfecta (OI) is a rare congenital disorder of the skeletal system, inflicting debilitating physical and psychological distress on patients and caregivers. Over the decades, much effort has been...

    Peikai Chen, Zhijia Tan, Anmei Qiu, Shijie Yin in Orphanet Journal of Rare Diseases (2022)