Publication:
Sturge Weber Syndrome – Roach’s Type II Variant

creativeworkseries.issnISSN 2091-0231 eISSN 2091-167X
dc.contributor.authorBista, Muna
dc.contributor.authorAgrawal, Sudha
dc.contributor.authorTaparia, Sweta
dc.date.accessioned2025-08-25T10:47:19Z
dc.date.available2025-08-25T10:47:19Z
dc.date.issued2020
dc.descriptionMuna Bista B.P. Koirala Institute of Health Sciences Sudha Agrawal B.P. Koirala Institute of Health Sciences, Dharan Sweta Taparia Taparia Eye Care Pvt Ltd, Biratnagar
dc.description.abstractAbstract: Sturge-Weber syndrome (SWS) is a neurocutaneous sporadic disorder caused by mutation in GNAQ gene responsible for persistence of vascular plexus around cephalic portion of neural tube. It has a wide spectrum of cutaneous, neurologic and ophthalmic manifestations, which may or may not be associated with one another. Roach scale has classified it into three types. Here, we present a case of Roach’s Type II variant of SWS with Port-wine stain (PWS) and ocular abnormalities without Central Nervous System (CNS) involvement. A 24 months old female presented with hemangioma involving the left side of face since birth. She had history of corneal edema and buphthalmos at two days of life. There was no history of seizure or developmental delay and Magnetic Resonance Imaging (MRI) of the head ruled out cranial hemangioma. Roach’s Type II is a rare variant of SWS and should be suspected in any case having PWS along the course of trigeminal nerve with congenital glaucoma because the neurologic involvement in a given case may vary from an absence to overt clinical manifestations with or without radiological changes. Due to its wide range of manifestations, a multidisciplinary approach is required for proper management of these patients. Keywords: Neural Tube, Neurocutaneous Syndromes, Port-Wine Stain, Sturge-Weber Syndrome
dc.identifierhttps://doi.org/10.3126/njdvl.v18i1.30316
dc.identifier.urihttps://hdl.handle.net/20.500.14572/2045
dc.language.isoen_US
dc.publisherSociety of Dermatologists, Venereologists and Leprologists of Nepal (SODVELON)
dc.titleSturge Weber Syndrome – Roach’s Type II Variant
dc.typeArticle
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage79
oaire.citation.startPage76
relation.isJournalIssueOfPublication8cee6379-b5d2-4085-b0d5-9d8f3bdda50f
relation.isJournalIssueOfPublication.latestForDiscovery8cee6379-b5d2-4085-b0d5-9d8f3bdda50f
relation.isJournalOfPublicationb2ab7aab-75b0-4bd1-9ed0-b8a91c68201a

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