Osteogenesis imperfecta · Group of genetic disorders resulting in fragile bones · YYNN

Osteogenesis imperfecta

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Group of genetic disorders resulting in fragile bones

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Beware of Osteogenesis Imperfecta: Subdural Hematoma in a 10-Year-Old Child With Minor Head Trauma

scientific article published on 01 July 2019

Mutations in FKBP10 cause both Bruck syndrome and isolated osteogenesis imperfecta in humans

Maternal and infant outcome after pamidronate treatment of polyostotic fibrous dysplasia and osteogenesis imperfecta before conception: a report of four cases

scientific article published on 21 March 2006

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Osteogenesis imperfecta (IPA: ; OI), colloquially known as brittle bone disease, is a group of genetic disorders that all result in bones that break easily. The range of symptoms—on the skeleton as well as on the body's other organs—may be mild to severe. Symptoms found in various types of OI include whites of the eye (sclerae) that are blue...

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designated intractable/rare disease

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