Literature DB >> 9114612

Dyschromatosis universalis hereditaria: an electron microscopic examination.

N S Kim1, S Im, S C Kim.   

Abstract

We report electron microscopic findings from both hyperchromic and achromic macules of dyschromatosis universalis hereditaria (DUH). The keratinocytes of the hyperchromic macules contained numerous, fully melanized melanosomes; almost all of them were aggregated to form the melanosome complex. In contrast, the melanosomes were absent from both keratinocytes and melanocytes of achromic macules, even though intact melanocytes were found. Our results suggest that DUH may be a disorder of melanosome production and distribution in epidermal melanin units rather than a a disorder of melanocyte number.

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Year:  1997        PMID: 9114612     DOI: 10.1111/j.1346-8138.1997.tb02764.x

Source DB:  PubMed          Journal:  J Dermatol        ISSN: 0385-2407            Impact factor:   4.005


  5 in total

1.  A Case of Sporadic Dyschromatosis Universalis Hereditaria.

Authors:  Je Min An; Bum Joon Ko; Moon Kyun Cho; Kyu Uang Whang
Journal:  Ann Dermatol       Date:  2015-07-29       Impact factor: 1.444

2.  [Dyschromatosis universalis hereditaria. An unusually rare clinical picture].

Authors:  I Elser; A S Hassan; J Rieker; T Ruzicka; M Megahed
Journal:  Hautarzt       Date:  2003-03-07       Impact factor: 0.751

3.  Adult onset dyschomatosis universalis.

Authors:  Min Sung Kim; Sang Ho Youn; Chan Ho Na; Bong Seok Shin
Journal:  Ann Dermatol       Date:  2015-02-03       Impact factor: 1.444

4.  Dyschromatosis universalis hereditaria with renal failure.

Authors:  Salinee Rojhirunsakool; Vasanop Vachiramon
Journal:  Case Rep Dermatol       Date:  2015-04-01

5.  A case of dyschromatosis universalis hereditaria with adermatoglyphia: A rare association.

Authors:  Sumir Kumar; Pritish Bhoyar; Bharat Bhushan Mahajan
Journal:  Indian Dermatol Online J       Date:  2015 Mar-Apr
  5 in total

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