The first comprehensive description of a syndrome comprisinglaxity and fragility of the skin associated with hypermobilityof the large joints was published in 1892 by Tschernogobow1in Moscow. With remarkable insight, he interpreted the causeof the phenotype as a systemic defect in connective tissue.However, as is common in medicine, those who came later areimmortalized in the eponym, in this case Ehlers2 and Danlos,3Danish and French dermatologists, respectively, who publishedtheir observations independently in the first decade of the20th century.
The familial nature of these clinical associations was demonstratedin 1949,4 and soon thereafter Jansen5. . . [Full Text of this Article]
References
Related Letters:
EhlersDanlos Syndrome Type IV
Barabas A. P., Pinto Y. M., Pals G., Zijlstra J. G., Tulleken J. E., Byers P. H., Schwarze U., Pepin M., Pyeritz R. E.
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Full Text
N Engl J Med 2000;
343:366-368, Aug 3, 2000.
Correspondence
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Barabas, A. P., Pinto, Y. M., Pals, G., Zijlstra, J. G., Tulleken, J. E., Byers, P. H., Schwarze, U., Pepin, M., Pyeritz, R. E.
(2000). Ehlers-Danlos Syndrome Type IV. NEJM
343: 366-368
[Full Text]