Publication:
Sturge Weber Syndrome: A Case Report

creativeworkseries.issnISSN 1990-7974 eISSN 1990-7982
dc.contributor.authorDevkota, S
dc.contributor.authorUpadhyay, S
dc.date.accessioned2026-06-04T10:31:33Z
dc.date.available2026-06-04T10:31:33Z
dc.date.issued2010
dc.descriptionS Devkota Medical Officer, Department of Paediatrics, Nepal Medical College and Teaching Hospital, Jorpati, Kathmandu S Upadhyay Lecturer, Department of Paediatrics, Nepal Medical College and Teaching Hospital, Jorpati, Kathmandu
dc.description.abstractAbstract: Sturge-Weber syndrome is a neurocutaneous syndrome characterized by port wine stain, congenital glaucoma, and underlying anomalous leptomeningeal venous plexus and the lack of normal cortical venous drainage. It is a congenital but not an inherited disease and it occurs sporadically and is very rare, incidence being approximately 1 on 50000. It occurs with rare exception but occasionally the other members of the family may have hemangiomata of a lesser degree.
dc.identifierhttps://doi.org/10.3126/jnps.v30i3.3920
dc.identifier.urihttps://hdl.handle.net/20.500.14572/6368
dc.language.isoen_US
dc.subjectSturge Weber Syndrome
dc.titleSturge Weber Syndrome: A Case Report
dc.typeArticle
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage165
oaire.citation.startPage164
relation.isJournalIssueOfPublication606d4588-8be5-4d11-88f9-29697ba6b4e4
relation.isJournalIssueOfPublication.latestForDiscovery606d4588-8be5-4d11-88f9-29697ba6b4e4
relation.isJournalOfPublication6f9be05c-05a9-4a3e-a5b5-a19a15ab042c

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