Camurati-Engelmann disease
Synonyms: Progressive diaphyseal dysplasia
Camurati-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. Camurati-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.
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.
Reference: Access aggregated data from Orphanet at Orphadata.
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version April 2024
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Camurati-Engelmann disease?
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Provide information, support and advocacy to families caring for a child with an undiagnosed or rare genetic condition.
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The Chandler Project brings awareness and shines a light on transformative research surrounding achondroplasia and other skeletal dysplasias by offering support to a global community and network of patients, parents, and caregivers seeking information on scientific discoveries, pharmaceutical advancements and surgical treatment options.
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