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Klippel-Trénaunay-Weber syndrome—report of a case associated with an incomplete form of Sturge-Weber syndrome
Authors:P. DONOFRIO  F. AYALA
Affiliation:Department of Dermatology, 2nd School of Medicine, University of Naples, Naples, Italy
Abstract:A 23-year-old man with angiomatous lesions on the left half of the body, varicose veins and hypertrophy of soft tissue and bone of the left upper limb is reported. Of particular interest was the association with angiomatous lesions on the left half of the face with visual disturbance. The combination of Klippel-Trénaunay-Weber syndrome and an incomplete form of Sturge-Weber syndrome could suggest a nosological relationship.
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