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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Detalles Bibliográficos
Autores principales: Moscote-Salazar, Luis Rafael, Koller, Osvaldo, Valenzuela, Sergio, Narvaez-Rojas, Alexis, Satyarthee, Guru D., Mo-Carrascal, Joulen, Maraby, Johana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6413607/
https://www.ncbi.nlm.nih.gov/pubmed/30937089
http://dx.doi.org/10.4103/JPN.JPN_9_18

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6413607/
https://www.ncbi.nlm.nih.gov/pubmed/30937089
http://dx.doi.org/10.4103/JPN.JPN_9_18

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