Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.14356/1721
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dc.contributor.authorSah, R K-
dc.contributor.authorGhimire, S-
dc.contributor.authorBagale, B B-
dc.contributor.authorKayastha, M-
dc.contributor.authorChapagain, R H-
dc.date.accessioned2023-05-19T06:25:17Z-
dc.date.available2023-05-19T06:25:17Z-
dc.date.issued2016-
dc.identifier.citationSahR. K., GhimireS., BagaleB. B., KayasthaM., & ChapagainR. H. (2016). Klippel-Trenaunay Syndrome: A Case Report. Journal of Nepal Health Research Council, 14(2). https://doi.org/10.33314/jnhrc.v14i2.804en_US
dc.identifier.issnPrint ISSN: 1727-5482; Online ISSN: 1999-6217-
dc.identifier.urihttp://103.69.126.140:8080/handle/20.500.14356/1721-
dc.descriptionCase Studyen_US
dc.description.abstractAbstract Klippel-Trenaunaysyndrome(KTS) is a rare congenital condition usually presenting with port wine stains, excessive growth of bones and soft tissue and varicose veins which most commonly occurs in the legs, but it also may affect the arms, face, head, or internal organs. We report a case of term male neonate with clinical findings of Port-wine stain, multiple cystic swellings with ultrasonographic findings suggestive of vascular malformations and limb abnormalities in the form ofsoft tissue hypertrophy of right upper limb, polydactyly of right hand and syndactyly of left hand consistent withKlippel-Trenaunay syndrome. Keywords: Klippel-trenaunay syndrome; port-wine stain, vascular malformations; soft tissue swelling;polydactyly.en_US
dc.language.isoenen_US
dc.publisherNepal Health Research Councilen_US
dc.relation.ispartofseriesMay-Aug, 2016;804-
dc.subjectKlippel-trenaunay syndromeen_US
dc.subjectport-wine stainen_US
dc.subjectVascular malformationsen_US
dc.subjectSoft tissue swellingen_US
dc.subjectPolydactylyen_US
dc.titleKlippel-Trenaunay Syndrome: A Case Reporten_US
dc.typeJournal Articleen_US
local.journal.categoryCase Study-
Appears in Collections:Vol. 14 No. 2 Issue 33 May-Aug 2016

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