Camurati-Engelmann disease : pictorial essay

Show simple item record Bellew, Neil Wagener, Georg 2011-03-08T06:31:36Z 2011-03-08T06:31:36Z 2011-03
dc.description.abstract Camurati-Engelmann disease (CED), or progressive diaphyseal dysplasia, is a rare sclerosing dysplasia of which 250 cases have been described in the English literature. The disease affects one in a million people and is autosomal dominant with variable penetrance. It was initially described by Cockayne in 1920; Camurati was the first to suggest its hereditary nature in 1922. A single case of muscular wasting and marked bone involvement was reported by Engelmann in 1929. As the name suggests, there is progressive hyperostosis and predominant involvement of the diaphyses. en_US
dc.identifier.citation Bellew, N & Wagener, G 2011, 'Camurati-Engelmann disease : pictorial essay', SA Journal of Radiology, vol. 15, no. 1, pp. 20-24. [] en_US
dc.identifier.issn 1027-202X
dc.language.iso en en_US
dc.publisher Health & Medical Publishing Group en_US
dc.rights Health & Medical Publishing Group en_US
dc.subject Steve Biko Academic Hospital (SBAH) en_US
dc.title Camurati-Engelmann disease : pictorial essay en_US
dc.type Article en_US

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