Literature DB >> 12437556

Dyschromatosis universalis hereditaria: report of a case and review of the literature.

Khalid Al Hawsawi1, Khalid Al Aboud, V Ramesh, Daifullah Al Aboud.   

Abstract

We describe dyschromatosis universalis in a 19-month-old Saudi Arabian girl. She had no associated defects and none of the other family members were affected. Similar cases reported from countries other than the Far East, where the disease was first described, are discussed.

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Mesh：

Year:  2002        PMID： 12437556     DOI： 10.1046/j.1525-1470.2002.00225.x

Source DB:  PubMed          Journal:  Pediatr Dermatol        ISSN： 0736-8046            Impact factor:   1.588


  12 in total

1.  Familial progressive hyper- and hypopigmentation: a report on a Chinese family and evidence for genetic heterogeneity.

Authors:  Fang Xiao-Kai; He Yue-Xi; Li Yan-Jia; Chen Li-Rong; Wang He-Peng; Sun Qing
Journal:  An Bras Dermatol       Date:  2017 May-Jun       Impact factor: 1.896

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.  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

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

6.  Differential Diagnosis of Two Chinese Families with Dyschromatoses by Targeted Gene Sequencing.

Authors:  Jia-Wei Liu; Jun Sun; Sergio Vano-Galvan; Feng-Xia Liu; Xiu-Xiu Wei; Dong-Lai Ma
Journal:  Chin Med J (Engl)       Date:  2016-01-05       Impact factor: 2.628

7.  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

8.  Dyschromatosis universalis hereditaria: Infrequent genodermatoses in India.

Authors:  Hari Kishan Kumar Yadalla; Srivalli Pinninti; Anagha Ramesh Babu
Journal:  Indian J Hum Genet       Date:  2013-10

9.  Genome-wide linkage, exome sequencing and functional analyses identify ABCB6 as the pathogenic gene of dyschromatosis universalis hereditaria.

Authors:  Hong Liu; Yi Li; Ken Kwok Hon Hung; Na Wang; Chuan Wang; Xuechao Chen; Donglai Sheng; Xi'an Fu; Kelvin See; Jia Nee Foo; Huiqi Low; Herty Liany; Ishak Darryl Irwan; Jian Liu; Baoqi Yang; Mingfei Chen; Yongxiang Yu; Gongqi Yu; Guiye Niu; Jiabao You; Yan Zhou; Shanshan Ma; Ting Wang; Xiaoxiao Yan; Boon Kee Goh; John E A Common; Birgitte E Lane; Yonghu Sun; Guizhi Zhou; Xianmei Lu; Zhenhua Wang; Hongqing Tian; Yuanhua Cao; Shumin Chen; Qiji Liu; Jianjun Liu; Furen Zhang
Journal:  PLoS One       Date:  2014-02-03       Impact factor: 3.240

10.  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
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