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Title: Phakomatosis pigmentovascularis type IIb associated with Sturge-Weber syndrome. Author: Al Robaee A, Banka N, Alfadley A. Journal: Pediatr Dermatol; 2004; 21(6):642-5. PubMed ID: 15575847. 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.[Abstract] [Full Text] [Related] [New Search]