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 CASE REPORT
Year : 2014  |  Volume : 80  |  Issue : 1  |  Page : 51--53

Sturge-Weber syndrome in association with Klippel-Trenaunay syndrome and phakomatosis pigmentovascularis type IIb


1 Department of Dermatology, Venereology, and Leprosy, North Bengal Medical College, Darjeeling, West Bengal, India
2 R G Kar Medical College, Kolkata, West Bengal, India
3 Department of Radiology, North Bengal Medical College, Darjeeling, West Bengal, India

Correspondence Address:
Rajesh Kumar Mandal
Department of Dermatology, Venereology, and Leprosy, North Bengal Medical College, Darjeeling - 734 012, West Bengal
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0378-6323.125507

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Phakomatosis pigmentovascularis (PPV) is a rare combination of pigmentary and vascular components with or without systemic involvement. We report here a rare association of Sturge-Weber syndrome, Klippel-Trenaunay syndrome, and PPV type IIb in a 15-year-old boy who had right upper limb monoparesis along with a history of recurrent convulsions.






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Online since 15th March '04
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