Neki N S.
Sturge Weber Syndrome-unusual presentation.
J Ayub Med Coll Abottabad Jan ;26(1):106-7.

Sturge Weber Syndrome or encephalo-trigeminal angiomatosis is non-hereditary, congenital and rare disorder of unknown aetiology. It is characterised by vascular malformation with capillary venous angiomas involving face, eye and leptomeninges resulting in neurological and orbital manifestations. A case of 23 years old female presented with history of tonic-clonic convulsions, evidence of Port wine stain on face since birth, characteristic CT findings diagnosed as a case of Sturge Weber Syndrome is reported here for its rarity

PakMediNet -Pakistan's largest Database of Pakistani Medical Journals - http://www.pakmedinet.com