European Journal of Dermatology
MENUUnilateral facial telangiectases suggest type 1 segmental manifestation of Osler‐Rendu‐Weber syndrome in an 11‐year‐old boy Volume 13, numéro 6, November - December 2003
Illustrations
Department of Dermatology and Allergology, University Clinic of the RWTH Aachen, Pauwelsstrasse 30, D‐52074 Aachen, Germany
- Mots-clés : cutaneous mosaicism, hereditary hemorrhagic telangiectasia, Osler‐Weber‐Rendu syndrome, segmental skin disorder, unilateral nevoid telangiectasia
- Page(s) : 537-9
- Année de parution : 2003
An 11‐year‐old boy revealed multiple telangiectases confined to the left cheek and the left side of the lips. Additionally, unilateral epistaxis was present. Radiological examinations of the brain, lungs and abdomen were normal and bleeding of the gastrointestinal tract was excluded. In this case, we propose a probable segmental type 1 manifestation of the autosomal dominantly inherited Osler‐Weber‐Rendu syndrome.