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Disease: Osteogenesis imperfecta- type 2B

  • ACVR2B/Fc counteracts chemotherapy-induced loss of muscle and bone mass
  • Administration of soluble activin receptor 2B increases bone and muscle mass in a mouse model of osteogenesis imperfecta
  • Anesthetic management of ventricular-peritoneal shunt implantation in osteogenesis imperfecta type IIB: A case report
  • Identification of a COL1A2 mutation with a deletion spanning coding and intronic sequence in exon 19 and intron 19 in a fetus with osteogenesis imperfecta type II
  • Mutation Analysis of COL1A1 and COL1A2 in Fetuses with Osteogenesis Imperfecta Type II/III
  • Osteogenesis imperfecta type II: prenatal diagnosis and association with increased nuchal translucency and hypoechogenicity of the cranium
  • Osteogenesis Imperfecta: New Perspectives From Clinical and Translational Research
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CheckOrphan is a non-profit organization located in Basel, Switzerland and Santa Cruz, California that is dedicated to rare, orphan and neglected diseases. CheckOrphan offers users an interactive and dynamic platform for all these diseases. This strategy allows visitors to be updated daily on all the latest news and interact with people internationally. This is essential, because due to the nature of these diseases, there is not a large concentration of individuals within any given proximity.
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