Publication: Waardenburg syndrome Type II
| creativeworkseries.issn | 1812-2027 | |
| dc.contributor.author | Singh, I | |
| dc.contributor.author | Maharjan, M | |
| dc.contributor.author | Gautam, DK | |
| dc.contributor.author | Mehar, R | |
| dc.contributor.author | Gathwala, G | |
| dc.date.accessioned | 2025-07-24T07:32:03Z | |
| dc.date.available | 2025-07-24T07:32:03Z | |
| dc.date.issued | 2006 | |
| dc.description | Singh I 1, Maharjan M 2, Gautam DK 3, Mehar R 4, Gathwala G 5 1Chief of ENT Unit, 2,3Residents ENT, 4Assistant Professor ENT, 5Professor, Paediatric Department of Otolaryngology & Head and Neck Surgery, B.P. Koirala Institute of Health Sciences, Dharan, Nepal. 4 Assistant Professor, Himalayan Institute of Medical Sciences, Dehradun, 5Professor of Paediatrics, Pt. Bhagawat Dayal Post Graduate Institute of Medical Sciences, Rohtak, India | |
| dc.description.abstract | Two rare cases of Waardenburg type II are reported. First case had three main features of WS-profound SN hearing loss, hetrochromia iris and white forelock of hair. Second case had moderate SNHL and depigmentation of hair. Key words: Hetrochromia iris, white forelock hair | |
| dc.identifier.uri | https://hdl.handle.net/20.500.14572/600 | |
| dc.language.iso | en_US | |
| dc.publisher | Kathmandu University | |
| dc.title | Waardenburg syndrome Type II | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
| local.article.type | Case Report | |
| oaire.citation.endPage | 509 | |
| oaire.citation.startPage | 506 | |
| relation.isJournalIssueOfPublication | 33ef012a-4a08-47e9-beb2-7862118d90bf | |
| relation.isJournalIssueOfPublication.latestForDiscovery | 33ef012a-4a08-47e9-beb2-7862118d90bf | |
| relation.isJournalOfPublication | a782b7ff-cf89-4178-ad1c-11ed89cfe1bd |