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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Detalles Bibliográficos
Autores principales: Chetty, Manogari, Roberts, Tina Sharon, Stephen, Lawrence, Beighton, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5831017/
https://www.ncbi.nlm.nih.gov/pubmed/29607091
http://dx.doi.org/10.1038/bdjopen.2017.21

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5831017/
https://www.ncbi.nlm.nih.gov/pubmed/29607091
http://dx.doi.org/10.1038/bdjopen.2017.21

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