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Klippel‐Trénaunay‐Weber syndrome—report of a case associated with an incomplete form of Sturge‐Weber syndrome
Author(s) -
DONOFRIO P.,
AYALA F.
Publication year - 1984
Publication title -
clinical and experimental dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.587
H-Index - 78
eISSN - 1365-2230
pISSN - 0307-6938
DOI - 10.1111/j.1365-2230.1984.tb00848.x
Subject(s) - sturge–weber syndrome , medicine , dermatology
Summary 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.