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Osteogenesis imperfecta (.mw-parser-output .IPA-label-small{font-size:85%}.mw-parser-output .references .IPA-label-small,.mw-parser-output .infobox .IPA-label-small,.mw-parser-output .navbox .IPA-label-small{font-size:100%}IPA: /ˌɒstioʊˈdʒɛnəsɪs ˌɪmpɜːrˈfɛktə/; OI), colloquially known as brittle bone disease, is a group of genetic disorders that all…
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oi type types may bone iii imperfecta genetic bones collagen mutations fractures severe iv cases cause patients osteogenesis also surgery
| Subject | Predicate | Object | Confidence | Src |
|---|---|---|---|---|
| Osteogenesis imperfecta | Causes | Genetic (autosomal dominant or de novo mutation) | 1.00 | infobox |
| Osteogenesis imperfecta | Diagnostic method | Based on symptoms, DNA testing | 1.00 | infobox |
| Osteogenesis imperfecta | Duration | Long term | 1.00 | infobox |
| Osteogenesis imperfecta | Frequency | 1 in 15,000–20,000 people | 1.00 | infobox |
| Osteogenesis imperfecta | Management | Healthy lifestyle (exercise, no smoking), metal rods through the long bones | 1.00 | infobox |
| Osteogenesis imperfecta | Medication | Bisphosphonates | 1.00 | infobox |
| Osteogenesis imperfecta | Onset | Birth | 1.00 | infobox |
| Osteogenesis imperfecta | Other names | Brittle bone disease, Lobstein syndrome,: 5 fragilitas ossium, Vrolik disease,: 5 osteopsathyrosis idiopathica: 347 | 1.00 | infobox |
| Osteogenesis imperfecta | Prevention | Pre-implantation genetic diagnosis | 1.00 | infobox |
| Osteogenesis imperfecta | Prognosis | Depends on the type | 1.00 | infobox |
| Osteogenesis imperfecta | Pronunciation | /ˌɒstioʊˈdʒɛnəsɪs ˌɪmpɜːrˈfɛktə/ OSS-tee-oh-JEN-ə-siss IM-pur-FEK-tə | 1.00 | infobox |
| Osteogenesis imperfecta | Specialty | Pediatrics, medical genetics, orthopedics | 1.00 | infobox |
| Osteogenesis imperfecta | Symptoms | Bones that break easily, blue tinge to the sclera (whites of the eye), short height, joint hypermobility, hearing loss | 1.00 | infobox |
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