Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9223958 | Annales de Dermatologie et de Vénéréologie | 2005 | 4 Pages |
Abstract
This case report raises doubt on the exclusively cutaneous nature of benign hereditary telangiectasic-type capillary malformations. Moreover, it illustrates the possibility of a particular clinical form of this affection, associating classical telangiectasia and post-wine stain-type macules. The recent localization of the locus implied in this affection in 5q14 in the same chromosomic space as the CMC1 locus incriminated in familial capillary malformations, suggests that these two affections are in fact phenotype variations of a single and same clinical entity.
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Authors
C. Puso, B. Guillot, L. Durand, J.-J. Guilhou, D. Bessis,