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Phakomatosis pigmentovascularis type IIb associated with Sturge-Weber syndrome
Ahmad Al Robaee1, Nusrat Banka, Abdullah Alfadley
1Department of Medicine, King Faisal Specialist Hospital and Research Center, Riyadh 11211, Saudi Arabia.
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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