OI written 18 times in different colors.RESEARCH

New OI-causing gene (KDELR2) detected

21/11/2020By

By Dr. Oliver Semler, Paediatrician, OIFE Medical Advisory Board (MAB) A new OI-gene has been detected by a European group of researchers from Germany, UK, The Netherlands and Spain. The new type of OI is inherited in a recessive way. In most individuals with Osteogenesis imperfecta, the disease is inherited in a dominant way and…

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Collage clinical imagesRESEARCH

Investigating Denosumab in children with OI

17/11/2020By

Clinical trial: Investigating Denosumab in children with OI Interview with Dr. Jörg Oliver Semler, Paediatrician, OIFE Medical Advisory Board (MAB) How did the project of investigating denosumab in children start? Regarding the use of denosumab in OI there are a few projects which have to be separated. At the beginning there were a few case…

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