Abstract:
:Sturge-Weber syndrome is a rare sporadic condition of mesodermal phakomatosis, characterized by purple-colored flat cutaneous cranial (face) hemangiomas (most commonly along the trigeminal nerve), glaucoma and vascular lesions in the ipsilateral brain and meninges. Klippel-Trenaunay syndrome is also an uncommon mesodermal phakomatosis characterized by a triad of cutaneous and visceral hemangiomas, venous varicosities and soft tissue or bone hypertrophy. Sturge-Weber syndrome in combination with Klippel-Trenaunay syndrome is unusual. Because of the rarity, we report here a 3-year-old boy who presented with overlapping features of both the syndromes.
journal_name
Indian J Dermatoljournal_title
Indian journal of dermatologyauthors
Purkait R,Samanta T,Sinhamahapatra T,Chatterjee Mdoi
10.4103/0019-5154.91848subject
Has Abstractpub_date
2011-11-01 00:00:00pages
755-7issue
6eissn
0019-5154issn
1998-3611pii
IJD-56-755journal_volume
56pub_type
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