Publication:
Sturge Weber Syndrome Overlapping with Klippel Trenaunay Syndrome

creativeworkseries.issnISSN 1990-7974 eISSN 1990-7982
dc.contributor.authorSarkar, Shatanik
dc.contributor.authorPatra, Chaitali
dc.contributor.authorDey, Chandrasekhar
dc.contributor.authorDasgupta, Malay Kumar
dc.contributor.authorKundu, Tapan Kumar
dc.date.accessioned2026-05-22T06:45:05Z
dc.date.available2026-05-22T06:45:05Z
dc.date.issued2013
dc.descriptionShatanik Sarkar R. G. Kar Medical College & Hospital Chaitali Patra R. G. Kar Medical College & Hospital Chandrasekhar Dey R. G. Kar Medical College & Hospital Malay Kumar Dasgupta R. G. Kar Medical College & Hospital Tapan Kumar Kundu R. G. Kar Medical College & Hospital
dc.description.abstractAbstract: Sturge Weber syndrome (SWS) is a mesodermal phakomatosis characterized by meningo-facial angiomas with cerebral calcification. Klippel Trenaunay syndrome (KTS) is another very rare type of phakomatosis with cutaneous angiomas, varicose veins and enlargement of soft tissue or bones. Overlap between SWS & KTS is very rarely encountered. We report a three and half year old girl with overlapping features of both SWS and KTS.
dc.identifierhttps://doi.org/10.3126/jnps.v33i2.7704
dc.identifier.urihttps://hdl.handle.net/20.500.14572/6200
dc.language.isoen_US
dc.publisherNepal Paediatric Society (JNPS)
dc.subjectSturge Weber syndrome
dc.subjectPort wine stain
dc.subjectHemihypertrophy
dc.subjectKlippel Trenaunay syndrome
dc.titleSturge Weber Syndrome Overlapping with Klippel Trenaunay Syndrome
dc.typeArticle
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage149
oaire.citation.startPage147
relation.isJournalIssueOfPublication358a10cd-ca61-43c3-a1a7-fccff54666de
relation.isJournalIssueOfPublication.latestForDiscovery358a10cd-ca61-43c3-a1a7-fccff54666de
relation.isJournalOfPublication6f9be05c-05a9-4a3e-a5b5-a19a15ab042c

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