Phakomatosis pigmentovascularis presenting with Sturge-Weber syndrome and Klippel-Trenaunay syndrome

Phakomatosis pigmentovascularis (PPV) is a rare cutaneous disorder characterized by combination of capillary malformation and other pigmented naevi. Four types and two subtypes have been described where subtype ′a′ present only with cutaneous form and subtype ′b′ also with systemic association like...

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Bibliographic Details
Main Authors: Sumit Sen, Sanchaita Bala, Chinmay Halder, Rahul Ahar, Anusree Gangopadhyay
Format: Article
Published: Wolters Kluwer Medknow Publications 2015-01-01
Series:Indian Journal of Dermatology
Online Access:;year=2015;volume=60;issue=1;spage=77;epage=79;aulast=Sen