Publication:
Dyschromatosis universalis hereditaria with renal failure

Issued Date

2015-01-01

Resource Type

Article

ISSN

16626567

DOI

10.1159/000381174

Other identifier(s)

2-s2.0-84929593657

Rights

Mahidol University

Rights Holder(s)

SCOPUS

Bibliographic Citation

Case Reports in Dermatology. Vol.7, No.1 (2015), 51-55

Suggested Citation

Salinee Rojhirunsakool, Vasanop Vachiramon Dyschromatosis universalis hereditaria with renal failure. Case Reports in Dermatology. Vol.7, No.1 (2015), 51-55. doi:10.1159/000381174 Retrieved from: https://repository.li.mahidol.ac.th/handle/123456789/36685

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Title

Dyschromatosis universalis hereditaria with renal failure

Author(s)

Salinee Rojhirunsakool
 Vasanop Vachiramon

Other Contributor(s)

Mahidol University

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.

Keyword(s)

Medicine

Availability

URI

https://repository.li.mahidol.ac.th/handle/123456789/36685

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Scopus 2011-2015