Publication: Dyschromatosis universalis hereditaria with renal failure
| dc.contributor.author | Salinee Rojhirunsakool | en_US |
| dc.contributor.author | Vasanop Vachiramon | en_US |
| dc.contributor.other | Mahidol University | en_US |
| dc.date.accessioned | 2018-11-23T10:58:26Z | |
| dc.date.available | 2018-11-23T10:58:26Z | |
| dc.date.issued | 2015-01-01 | en_US |
| dc.description.abstract | © 2015 S. Karger AG, Basel. Dyschromatosis universalis hereditaria (DUH) is a rare autosomal dominant inherited dermatosis which usually appears during childhood and is characterized by dyspigmentation, with both hypopigmented and hyperpigmented macules. We report a case of DUH with unexplained childhood-onset renal failure. The association between DUH and renal failure is yet to be proven by further studies. | en_US |
| dc.identifier.citation | Case Reports in Dermatology. Vol.7, No.1 (2015), 51-55 | en_US |
| dc.identifier.doi | 10.1159/000381174 | en_US |
| dc.identifier.issn | 16626567 | en_US |
| dc.identifier.other | 2-s2.0-84929593657 | en_US |
| dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/123456789/36685 | |
| dc.rights | Mahidol University | en_US |
| dc.rights.holder | SCOPUS | en_US |
| dc.source.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84929593657&origin=inward | en_US |
| dc.subject | Medicine | en_US |
| dc.title | Dyschromatosis universalis hereditaria with renal failure | en_US |
| dc.type | Article | en_US |
| dspace.entity.type | Publication | |
| mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84929593657&origin=inward | en_US |