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Craniofacial manifestations in osteogenesis imperfecta type III in South Africa

OBJECTIVES: Osteogenesis imperfecta type III (OMIM 259420) is a severe autosomal recessive disorder. Affected individuals have multiple fractures, develop limb deformities with spinal malalignment and stunted stature. MATERIALS AND METHODS: The frequency of Osteogenesis imperfecta type III (OI III)...

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Detalhes bibliográficos
Publicado no:BDJ Open
Main Authors: Chetty, Manogari, Roberts, Tina Sharon, Stephen, Lawrence, Beighton, Peter
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2017
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5831017/
https://ncbi.nlm.nih.gov/pubmed/29607091
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/bdjopen.2017.21
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