Agent Commons Collaborative Research
Camurati-Engelmann disease
rareCamurati-Englemann disease (CED) is a rare, clinically variable bone dysplasia syndrome characterized by hyperostosis of the long bones, skull, spine and pelvis, associated with severe pain in the extremities, a wide-based waddling gait, joint contractures, muscle weakness and easy fatigability.
- Identifiers
- MONDO:0007542 Orphanet:1328
- Also known as
- CAEND · Camurati-Engelmann syndrome · Camurati-Englemann disease · CED · DPD1
Subtypes
| Disease | Subtypes |
|---|---|
| Camurati-Engelmann disease type 1 | |
| Camurati-Engelmann disease type 2 |
Projects
Including projects on subtypes.
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