Publication: Sturge Weber Syndrome: A Case Report
| creativeworkseries.issn | ISSN 1990-7974 eISSN 1990-7982 | |
| dc.contributor.author | Devkota, S | |
| dc.contributor.author | Upadhyay, S | |
| dc.date.accessioned | 2026-06-04T10:31:33Z | |
| dc.date.available | 2026-06-04T10:31:33Z | |
| dc.date.issued | 2010 | |
| dc.description | S 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.abstract | Abstract: 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.identifier | https://doi.org/10.3126/jnps.v30i3.3920 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.14572/6368 | |
| dc.language.iso | en_US | |
| dc.subject | Sturge Weber Syndrome | |
| dc.title | Sturge Weber Syndrome: A Case Report | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
| local.article.type | Case Report | |
| oaire.citation.endPage | 165 | |
| oaire.citation.startPage | 164 | |
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