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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Bibliographische Detailangaben
Veröffentlicht in:J Pediatr Neurosci
Hauptverfasser: Moscote-Salazar, Luis Rafael, Koller, Osvaldo, Valenzuela, Sergio, Narvaez-Rojas, Alexis, Satyarthee, Guru D., Mo-Carrascal, Joulen, Maraby, Johana
Format: Artigo
Sprache:Inglês
Veröffentlicht: Medknow Publications & Media Pvt Ltd 2018
Schlagworte:
Case Report
Online Zugang: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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