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Review
. 2010 May-Jun;27(3):303-5.
doi: 10.1111/j.1525-1470.2010.01144.x.

Two reports of phacomatosis pigmentovascularis type IIb, one in association with Sturge-Weber syndrome and Klippel-Trenaunay syndrome

Lindsey B Finklea  1 , Melinda R Mohr, Molly M Warthan, David H Darrow, Judith V Williams
Affiliations
Review

Two reports of phacomatosis pigmentovascularis type IIb, one in association with Sturge-Weber syndrome and Klippel-Trenaunay syndrome

Lindsey B Finklea et al. Pediatr Dermatol. 2010 May-Jun.

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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