Winkelriedstrasse 10, Dermatology FMH, CH-5430 Wettingen SwitzerlandFax: (+41) 56 427 00 12., Department of Dermatology, University Hospital Maastricht, P. Debyelaan 25, PO Box 5800, 6202 AZ Maastricht, The Netherlands, Department of Dermatology, University of Basel, Department of Dermatology, Kantonsspital Aarau, Petersgraben 4, CH-4031 Basel Switzerland
- Mots-clés : monozygotic twins, Klippel-Trenaunay syndrome, postzygotic mutation, loss of heterozygosity, paradominant inheritance, genetic mosaicism
- Page(s) : 341-3
- Année de parution : 2005
Klippel-Trenaunay-syndrome (KTS) (OMIM 149000) is a congenital slow-flow capillary lymphaticovenous malformation often affecting the lower extremities and accompanied by bone and soft tissue hypertrophy. The cutaneous lesions are always surrounded by regions of unaffected skin in a mosaic pattern. Usually, KTS occurs sporadically but rare reports of familial segregation exist, contributing to the ongoing debate on the issue of heredity in this disease. Herein, we report on identical monozygotic male twins discordant for KTS. This observation strongly supports the model of paradominant inheritance that was recently proposed for this and similar disorders.