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Review
. 2004 Nov-Dec;21(6):642-5.
doi: 10.1111/j.0736-8046.2004.21605.x.

Phakomatosis pigmentovascularis type IIb associated with Sturge-Weber syndrome

Affiliations
Review

Phakomatosis pigmentovascularis type IIb associated with Sturge-Weber syndrome

Ahmad Al Robaee et al. Pediatr Dermatol. 2004 Nov-Dec.

Abstract

We describe a 23-month-old child with phakomatosis pigmentovascularis type IIb associated with Sturge-Weber syndrome. Phakomatosis pigmentovascularis type IIb is a rare cutaneous malformation characterized by the simultaneous occurrence of nevus flammeus and melanocytic nevi. A brief review of the literature is presented and classification of this rare disease is discussed.

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