| dc.contributor.author | Koley, Sankha | en_US |
| dc.contributor.author | Salodkar, Atul | en_US |
| dc.contributor.author | Saoji, Vikrant | en_US |
| dc.contributor.author | Choudhary, Sanjiv | en_US |
| dc.date.accessioned | 1399-07-09T06:21:51Z | fa_IR |
| dc.date.accessioned | 2020-09-30T06:21:51Z | |
| dc.date.available | 1399-07-09T06:21:51Z | fa_IR |
| dc.date.available | 2020-09-30T06:21:51Z | |
| dc.date.issued | 2009-12-01 | en_US |
| dc.date.issued | 1388-09-10 | fa_IR |
| dc.identifier.citation | Koley, Sankha, Salodkar, Atul, Saoji, Vikrant, Choudhary, Sanjiv. (2009). Piebaldism and Vitiligo in Two Brothers. Iranian Journal of Dermatology, 12(3), 8-11. | en_US |
| dc.identifier.issn | 2717-0721 | |
| dc.identifier.uri | http://iranjd.ir/article_101336.html | |
| dc.identifier.uri | https://iranjournals.nlai.ir/handle/123456789/300796 | |
| dc.description.abstract | <span>Piebaldism is an autosomal dominant uncommon (<1 in 20,000) congenital pigmentary disorder. Depigmented patches are present since birth. They usually remain unchanged throughout life. Vitiligo is its closest differential diagnosis. We report a unique family in which these two dissimilar depigmentations, i.e. piebaldism and vitiligo (with nevus depigmentosus), were noted in two brothers. To the best of our knowledge, this is the first report of this presentation in the literature.</span> | en_US |
| dc.format.extent | 450 | |
| dc.format.mimetype | application/pdf | |
| dc.language | English | |
| dc.language.iso | en_US | |
| dc.publisher | Iranian Society of Dermatology | en_US |
| dc.relation.ispartof | Iranian Journal of Dermatology | en_US |
| dc.subject | piebaldism | en_US |
| dc.subject | Vitiligo | en_US |
| dc.subject | depigmentation | en_US |
| dc.title | Piebaldism and Vitiligo in Two Brothers | en_US |
| dc.type | Text | en_US |
| dc.type | Case Report | en_US |
| dc.citation.volume | 12 | |
| dc.citation.issue | 3 | |
| dc.citation.spage | 8 | |
| dc.citation.epage | 11 | |
