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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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Dettagli Bibliografici
Pubblicato in:J Pediatr Neurosci
Autori principali: Moscote-Salazar, Luis Rafael, Koller, Osvaldo, Valenzuela, Sergio, Narvaez-Rojas, Alexis, Satyarthee, Guru D., Mo-Carrascal, Joulen, Maraby, Johana
Natura: Artigo
Lingua:Inglês
Pubblicazione: Medknow Publications & Media Pvt Ltd 2018
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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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