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Neurosurgical Implications of Osteogenesis Imperfecta in a Child after Fall: Case Illustration
Osteogenesis imperfecta (OI) is a group of hereditary genetic pathologies of connective tissue, which is characterized by bone fragility and fractures. It is classified into types I, II, III, IV, V, and VI. The disorder is caused by an autosomal-dominant mutation in one of the two genes that encode...
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| Pubblicato in: | J Pediatr Neurosci |
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| Autori principali: | , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Medknow Publications & Media Pvt Ltd
2018
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6413607/ https://ncbi.nlm.nih.gov/pubmed/30937089 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/JPN.JPN_9_18 |
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