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

RajeshKumar Mandal | Zendy; AsitChandra Roy | Zendy; SudipKumar Ghosh | Zendy; Sankha Koley | Zendy

AI Assistant Blog Pricing

Home ZAIA Blog

Open Access

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

Author(s) -

RajeshKumar Mandal,

AsitChandra Roy,

SudipKumar Ghosh,

Sankha Koley

Publication year - 2014

Publication title -

indian journal of dermatology venereology and leprology

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.514

H-Index - 45

eISSN - 0973-3922

pISSN - 0378-6323

DOI - 10.4103/0378-6323.125507

Subject(s) - klippel trenaunay syndrome , medicine , sturge–weber syndrome , dermatology , pathology , soft tissue

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.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.

Having issues? You can contact us here

Accelerating Research