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). The skull bones may be thickened so that the passages th...
<radiology> Sclerosing diaphyseal dysplasia, does not involve metaphysis, epiphysis, or bone marrow cavity Cf: Albers-Schoenberg disease ... (12 Dec 1998) ... 
(kah-moo-rah´te eng´gәl-mahn) diaphyseal dysplasia.
Type: Term Pronunciation: kah-mū-rah′tē-en′gĕl-mahn Synonyms: diaphysial dysplasia