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Camurati–Engelmann disease: a case report from sub-Saharan Africa
Camurati–Engelmann disease is a rare autosomal dominant inherited condition belonging to the group of craniotubular hyperostosis with characteristic radiological features of the diaphyses of the long bones and the skull. A 35-year-old female is reported presenting with bone pain and waddling gait, s...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Oxford University Press
2018
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6049015/ https://www.ncbi.nlm.nih.gov/pubmed/30034812 http://dx.doi.org/10.1093/omcr/omy036 |