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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Bibliografiske detaljer
Udgivet i:Oxf Med Case Reports
Main Authors: Mwasamwaja, Amos O, Mkwizu, Elifuraha W, Shao, Elichilia R, Kalambo, Clement F, Lyaruu, Isaack, Hamel, Ben C
Format: Artigo
Sprog:Inglês
Udgivet: Oxford University Press 2018
Fag:
Case Report
Online adgang: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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