Publication:
Sturge-Weber Syndrome: A Case Report

creativeworkseries.issnJNMA Print ISSN: 0028-2715; Online ISSN: 1815-672X
dc.contributor.authorTimilsina, Sunil
dc.contributor.authorKunwor, Bishal
dc.contributor.authorChhetri, Suchit Thapa
dc.contributor.authorNepal, Sanath
dc.contributor.authorSedhai, Khusbu
dc.date.accessioned2025-08-22T04:54:12Z
dc.date.available2025-08-22T04:54:12Z
dc.date.issued2023
dc.descriptionAuthors Sunil Timilsina Department of General Practice and Emergency Medicine, Shree Birendra Hospital, Chhauni, Kathmandu, Nepal Bishal Kunwor Nepalese Army Institute of Health Sciences, Sanobharyang, Kathmandu, Nepal Suchit Thapa Chhetri Nepalese Army Institute of Health Sciences, Sanobharyang, Kathmandu, Nepal Sanath Nepal Department of General Practice and Emergency Medicine, Shree Birendra Hospital, Chhauni, Kathmandu, Nepal Khusbu Sedhai Department of Internal Medicine, Manmohan Cardiothoracic Center, Maharajgunj, Kathmandu, Nepal
dc.description.abstractAbstract Sturge-Weber syndrome is a rare congenital neurocutaneous syndrome with an incidence of 1 in 50000 characterised by facial capillary malformation and vascular anomalies in the brain and eye. We present the case of a five-year-old child diagnosed with Sturge-Weber syndrome. The patient exhibited high-grade fever, headaches, and generalized tonic-clonic seizures. The history revealed a port-wine stain on the face and a history of seizures from the age of four months. Diagnostic imaging confirmed the presence of leptomeningeal vascular malformation, calcification in the brain, and abnormal electroencephalogram patterns, establishing the diagnosis of Sturge-Weber syndrome. Treatment with antiepileptic drugs led to seizure control. This case underscores the importance of early diagnosis and tailored treatment strategies for patients with Sturge-Weber syndrome.
dc.identifierhttps://doi.org/10.31729/jnma.8344
dc.identifier.urihttps://hdl.handle.net/20.500.14572/1911
dc.language.isoen_US
dc.publisherNepal Medical Association
dc.titleSturge-Weber Syndrome: A Case Report
dc.typeOther
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage892
oaire.citation.startPage890
relation.isJournalIssueOfPublication9380e6f7-494d-40b2-a2ce-3f02ecf3b957
relation.isJournalIssueOfPublication.latestForDiscovery9380e6f7-494d-40b2-a2ce-3f02ecf3b957
relation.isJournalOfPublicatione6e146a0-0ece-4aba-aa0a-6ccfbd10a12a

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