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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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Détails bibliographiques
Publié dans:J Pediatr Neurosci
Auteurs principaux: Moscote-Salazar, Luis Rafael, Koller, Osvaldo, Valenzuela, Sergio, Narvaez-Rojas, Alexis, Satyarthee, Guru D., Mo-Carrascal, Joulen, Maraby, Johana
Format: Artigo
Langue:Inglês
Publié: Medknow Publications & Media Pvt Ltd 2018
Sujets:
Accès en ligne: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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