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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...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Oxf Med Case Reports |
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| Κύριοι συγγραφείς: | , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Oxford University Press
2018
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6049015/ https://ncbi.nlm.nih.gov/pubmed/30034812 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/omcr/omy036 |
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