Literature DB >> 16684309

Dyschromatosis universalis hereditaria as an autosomal recessive disease in five members of one family.

I A Bukhari, E A El-Harith, M Stuhrmann.   

Abstract

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Year:  2006        PMID： 16684309     DOI： 10.1111/j.1468-3083.2006.01522.x

Source DB:  PubMed          Journal:  J Eur Acad Dermatol Venereol        ISSN： 0926-9959            Impact factor:   6.166


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  10 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.  Mutations in POFUT1, encoding protein O-fucosyltransferase 1, cause generalized Dowling-Degos disease.

Authors:  Ming Li; Ruhong Cheng; Jianying Liang; Heng Yan; Hui Zhang; Lijia Yang; Chengrang Li; Qingqing Jiao; Zhiyong Lu; Jianhui He; Jin Ji; Zhu Shen; Chunqi Li; Fei Hao; Hong Yu; Zhirong Yao
Journal:  Am J Hum Genet       Date:  2013-05-16       Impact factor: 11.025

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.  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.  De novo mutation in KITLG gene causes a variant of Familial Progressive Hyper- and Hypo-pigmentation (FPHH).

Authors:  Mario Gorenjak; Nino Fijačko; Pij Bogomir Marko; Milanka Živanović; Uroš Potočnik
Journal:  Mol Genet Genomic Med       Date:  2021-10-30       Impact factor: 2.183

6.  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

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.  Reticulate dermatoses.

Authors:  Keshavmurthy A Adya; Arun C Inamadar; Aparna Palit
Journal:  Indian J Dermatol       Date:  2014-01       Impact factor: 1.494

9.  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

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
  10 in total

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