Invited Historical Comment
Further diagnostic thoughts about the elephant man
Article first published online: 3 JUN 2005
DOI: 10.1002/ajmg.1320290407
Copyright © 1988 Wiley-Liss, Inc., A Wiley Company
Additional Information
How to Cite
Cohen, M. M., Optiz, J. M. and Reynolds, J. F. (1988), Further diagnostic thoughts about the elephant man. Am. J. Med. Genet., 29: 777–782. doi: 10.1002/ajmg.1320290407
Publication History
- Issue published online: 3 JUN 2005
- Article first published online: 3 JUN 2005
- Manuscript Revised: 9 NOV 1987
- Manuscript Received: 16 MAY 1987
- Abstract
- References
- Cited By
Keywords:
- neurofibromatosis von Recklinghausen;
- sporadic occurrence;
- Proteus syndrome
Abstract
Further evidence for a diagnosis of the Elephant Man's condition is reviewed. It is known that the Elephant Man had “mocassin” lesions, hyperostoses of the skull, and absence of café-au-lait spots, all of which are characteristic of Proteus syndrome. Recently, questions have been raised about his skeletal findings and their relevance to neurofibromatosis. However, other skeletal diagnoses have been entertained, including Maffucci syndrome, Paget's disease of bone, pyarthrosis, and fibrous dysplasia. These diagnostic possibilities are discussed and evaluated critically. It is concluded that the skeletal findings are most consistent with Proteus syndrome and coincidental hip disease secondary to childhood trauma.

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