Literature DB >> 19570083

Dyschromatosis universalis hereditaria in a young Nigerian female.

S M Yusuf1, M S Mijinyawa, M B Maiyaki, A Z Mohammed.   

Abstract

Dyschromatosis universalis hereditaria (DUH) is a clinically heterogeneous disorder that shows generalized mottled pigmentation. It occurs most commonly in Japanese persons, with sporadic reports from South Africa, India, and Iraq. Histopathology reveals a variable degree of pigmentary incontinence. Although the precise etiology of this disorder is not yet known, the clinicopathological findings implicate an inherent abnormality of melanosomes or melanin processing. We describe a case in a young Nigerian girl.

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Year:  2009        PMID: 19570083     DOI: 10.1111/j.1365-4632.2009.03290.x

Source DB:  PubMed          Journal:  Int J Dermatol        ISSN: 0011-9059            Impact factor:   2.736


  4 in total

1.  Photoletter to the editor: Dyschromatosis universalis hereditaria: an infrequently occurring entity in Europe.

Authors:  Nayra Merino de Paz; Marina Rodríguez-Martin; Patricia Contreras Ferrer; Maria Pestana-Eliche; Antonio Martin-Herrera; Antonio Noda-Cabrera
Journal:  J Dermatol Case Rep       Date:  2012-09-28

2.  A novel mutation in ABCB6 associated with dyschromatosis universalis hereditaria in a Saudi family.

Authors:  Sara Aldokhayel; Alballa Nouf; Aleedan Khalid; Alsaif Faisal; Alotaibi Maram; Alhumidi Ahmed; Alsaif Fahad
Journal:  JAAD Case Rep       Date:  2021-11-25

3.  Novel mutations of ABCB6 associated with autosomal dominant dyschromatosis universalis hereditaria.

Authors:  Ying-Xia Cui; Xin-Yi Xia; Yang Zhou; Lin Gao; Xue-Jun Shang; Tong Ni; Wei-Ping Wang; Xiao-Buo Fan; Hong-Lin Yin; Shao-Jun Jiang; Bing Yao; Yu-An Hu; Gang Wang; Xiao-Jun Li
Journal:  PLoS One       Date:  2013-11-05       Impact factor: 3.240

4.  Removal of forearm lentigines in dyschromatosis universalis hereditaria with a 755-nm Q-switched alexandrite laser.

Authors:  Yiming Li; Li Li
Journal:  JAAD Case Rep       Date:  2017-12-20
  4 in total

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