Camurati–Engelmann disease (CED) is a very rare autosomal dominant genetic disorder that causes characteristic anomalies in the skeleton. It is a form of dysplasia. Patients typically have heavily thickened bones especially along the shafts of the long bones (called diaphyseal dysplasia).
This page contains content from the copyrighted Wikipedia article "Camurati–Engelmann disease"; that content is used under the GNU Free Documentation License (GFDL). You may redistribute it, verbatim or modified, providing that you comply with the terms of the GFDL.