Explore: Osteogenesis

Osteogenesis imperfecta (IPA: /ˌɒstioʊˈdʒɛnəsɪs ˌɪmpɜːrˈfɛktə/; OI), colloquially known as brittle bone disease, is a group of genetic disorders that all

Distraction osteogenesis (DO), also called callus distraction, callotasis and osteodistraction, is a process used in orthopedic surgery, podiatric surgery

collagen type I cause the commonest inherited disorder of bone, called osteogenesis imperfecta. Minor, but important, amounts of small proteins, including

Ossification (also called osteogenesis or bone mineralization) in bone remodeling is the process of laying down new bone material by cells named osteoblasts

Brien M.; Morello, Roy (2020-10-01). "Management of Endocrine Disease: Osteogenesis imperfecta: an update on clinical features and therapies". European Journal

cause of osteogenesis imperfecta in the vast majority of perinatally lethal osteogenesis imperfecta, and progressively deforming osteogenesis imperfecta

number of conditions, including transverse myelitis, Behçet disease, osteogenesis imperfecta, trauma, radiation myelopathy, vitamin B12 deficiency (subacute

diagnosis of brittle bone disease: osteogenesis imperfecta. Wormian bones may also be seen in: Pycnodysostosis Osteogenesis imperfecta Rickets "Kinky-hair"

type Osteoectasia familial Osteogenesis Imperfecta Osteogenesis imperfecta congenita microcephaly and cataracts Osteogenesis imperfecta congenital joint

active osteoblasts), and osteogenesis (living bone cells in the graft material contribute to bone remodeling). Osteogenesis only occurs with autograft