Literature DB >> 21382285

Dyschromatosis universalis hereditaria: a case report.

Carounanidy Udayashankar1, Amiya Kumar Nath.   

Abstract

Dyschromatosis universalis hereditaria (DUH) is usually an autosomal dominantly inherited disorder characterized by the presence of hypopigmented as well as hyperpigmented macules. We report an Indian patient with DUH with widespread involvement of skin including the face, oral mucous membranes (including tongue), and palms and soles. Our patient also exhibited nail changes, involvement of scalp hair, and keratosis pilaris.

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Year:  2011        PMID: 21382285

Source DB:  PubMed          Journal:  Dermatol Online J        ISSN: 1087-2108


  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.  Two novel SASH1 mutations in Chinese families with dyschromatosis universalis hereditaria.

Authors:  Jia-Wei Liu; Xiaerbati Habulieti; Rong-Rong Wang; Dong-Lai Ma; Xue Zhang
Journal:  J Clin Lab Anal       Date:  2021-05-24       Impact factor: 2.352

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.  Dyschromias: A Series of Five Interesting Cases from India.

Authors:  Prabhu Namitha; S Sacchidanand
Journal:  Indian J Dermatol       Date:  2015 Nov-Dec       Impact factor: 1.494

  4 in total

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