Sturge-Weber syndrome in association with Klippel-Trenaunay syndrome and phakomatosis pigmentovascularis type IIb.
Indian J Dermatol Venereol Leprol
;
2014 Jan-Feb; 80(1): 51-53
Article
in English
| IMSEAR
| ID: sea-154749
ABSTRACT
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.
Full text:
Available
Index:
IMSEAR (South-East Asia)
Main subject:
Phenotype
/
Pigmentation Disorders
/
Humans
/
Male
/
Sturge-Weber Syndrome
/
Adolescent
/
Klippel-Trenaunay-Weber Syndrome
/
Port-Wine Stain
Language:
English
Journal:
Indian J Dermatol Venereol Leprol
Year:
2014
Type:
Article
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