Camurati-Engelmann Disease: A rare genetic connective tissue disorder characterized by diaphyseal dysplasia, muscle weakness and leg pain. More detailed information about the symptoms, causes, and treatments of Camurati-Engelmann Disease is available below.
See full list of 37 symptoms of Camurati-Engelmann Disease
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Progressive thickening of diaphyseal cortex of long bones. - (Source - Diseases Database)
Camurati-Engelmann Disease is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Camurati-Engelmann Disease, or a subtype of Camurati-Engelmann Disease,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Camurati-Engelmann Disease as a "rare disease".
Source - Orphanet
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