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...

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Detalles Bibliográficos
Autores principales: Mwasamwaja, Amos O, Mkwizu, Elifuraha W, Shao, Elichilia R, Kalambo, Clement F, Lyaruu, Isaack, Hamel, Ben C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Case Report
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

Internet

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

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