Incontinentia pigmenti and Behçet´s syndrome: an unusual combination
DOI:
https://doi.org/10.2340/0001555566351354Abstract
We describe an unusual case of a child who had had incontinentia pigmenti from birth and developed the clinical picture of Beh√ßet´s syndrome at five years of age. Among the various investigations performed, chemotactic activity of the polymorphonuclear leukocyte was found to be low. We discuss the possibility that there are common immunological abnormalities in the two syndromes.Downloads
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Published
1986-07-01
How to Cite
Menni, S., Piccinno, R., Biolchini, A., Delle Piane, R., & Bardare, M. (1986). Incontinentia pigmenti and Behçet´s syndrome: an unusual combination. Acta Dermato-Venereologica, 66(4), 351–354. https://doi.org/10.2340/0001555566351354
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Copyright (c) 1986 Acta Dermato-VenereologicaAll digitalized ActaDV contents is available freely online. The Society for Publication of Acta Dermato-Venereologica owns the copyright for all material published until volume 88 (2008) and as from volume 89 (2009) the journal has been published fully Open Access, meaning the authors retain copyright to their work.
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