ba0006p131 | (1) | ICCBH2017
Moylan Alex
, Wakeling Emma L.
, Mughal M. Zulf
, Keen Richard
, Thornton Matt
, Peeva Daniela
, Jacobs Benjamin
Background: Camurati-Engelmann disease (CED) is a rare bone dysplasia characterised by hyperostosis and sclerosis of the diaphyses of the long bones and skull. It is caused by autosomal dominant gain-of function mutations within TGFB1, which result in increased activity of transforming growth factor β1 (TGF-β1). It typically presents in mid-childhood with bone pain, myopathy and progressive immobility. Evidence for treatment is based on a number of case repo...