Other Names for this Disease
- Diaphyseal dysplasia 1, progressive
- Engelmann disease
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On this page
- Camurati engelmann disease. Orphanet. February 2005; http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=1328. Accessed 4/17/2008.
- Katrien Janssens, Wendy Ballemans, Wim Van Hul. Camurati-Engelmann Disease. NORD Guide to Rare Disorders. 2003; Accessed 4/17/2008.
- Stephanie E Wallace, William R Wilcox. Camurati-Engelmann Disease. GeneReviews. August 16, 2006; http://www.genetests.org/query?dz=ced. Accessed 4/17/2008.
- GeneReviews provides current, expert-authored, peer-reviewed, full-text articles describing the application of genetic testing to the diagnosis, management, and genetic counseling of patients with specific inherited conditions. Click on the link to view the article on this topic.
- ClinicalTrials.gov lists trials that are studying or have studied Camurati-Engelmann disease. Click on the link to go to ClinicalTrials.gov to read descriptions of these studies.
- The U.S. National Institutes of Health, through the National Library of Medicine, developed ClinicalTrials.gov to provide patients, family members, and members of the public with current information on clinical research studies. There is a study titled Evaluation and Treatment of Skeletal Diseases which may be of interest to you.
- Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge.