2017
DOI: 10.22192/ijcrms.2017.03.03.001
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A case report on Sturge Weber Syndrome Seizures with Stain

Abstract: Sturge Weber Syndrome or encephalotrigeminal angiomatosis is non hereditary, congenital and rare disorder of unknown etiology. It is characterised by vascular malformation with capillary venous angiomas involving face, eye and leptomeninges resulting in neurological and orbital manifestations. A case of 46 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 … Show more

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“…A similar growth of Aspergillus spps. has been noted in immunocompetent patients in the studies of Tahir et al, Camus et al, Avkan-Oğuz et al, and Neki et al 2 8 9 10…”
Section: Discussionmentioning
confidence: 81%
“…A similar growth of Aspergillus spps. has been noted in immunocompetent patients in the studies of Tahir et al, Camus et al, Avkan-Oğuz et al, and Neki et al 2 8 9 10…”
Section: Discussionmentioning
confidence: 81%