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  • Title: Two reports of phacomatosis pigmentovascularis type IIb, one in association with Sturge-Weber syndrome and Klippel-Trenaunay syndrome.
    Author: Finklea LB, Mohr MR, Warthan MM, Darrow DH, Williams JV.
    Journal: Pediatr Dermatol; 2010; 27(3):303-5. PubMed ID: 20609155.
    Abstract:
    We present two rare cases of phacomatosis pigmentovascularis type IIb, with one patient demonstrating concurrent Sturge-Weber syndrome and Klippel-Trenaunay syndrome. To the best of our knowledge, this is the second infantile case meeting diagnostic criteria for systemic phacomatosis pigmentovascularis type IIb, Sturge-Weber syndrome and Klippel-Trenaunay syndrome in the English language literature.
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