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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...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | J Pediatr Neurosci |
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| Κύριοι συγγραφείς: | , , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Medknow Publications & Media Pvt Ltd
2018
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| Θέματα: | |
| Διαθέσιμο 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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