Intracranial variant of encephalotrigeminal angiomatosis – A case report

Encephalotrigeminal angiomatosis, also called Sturge–Weber syndrome (SWS), is a syndrome of etiology which is not yet clear. It is a nonhereditary condition. The clinical features include pigmentation over the facial skin known as port-wine stain, abnormalities of ocular region, and central nervous system involvement as leptomeningeal angioma. In this manuscript, we present a rare case report with an unusual combination of SWS with facial lobular capillary hemangioma.

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Encephalotrigeminal angiomatosis with facial lobular capillary hemangioma: An unusual case report

Karagir¹,

Adaki²,

Magdum³

2021

Int J App Basic Med Res

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Intracranial variant of encephalotrigeminal angiomatosis – A case report

Cited by 1 publication

References 14 publications

Encephalotrigeminal angiomatosis with facial lobular capillary hemangioma: An unusual case report

Encephalotrigeminal angiomatosis with facial lobular capillary hemangioma: An unusual case report

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