Literature DB >> 15482301

Dowling-Degos disease with dyschromatosis universalis hereditaria-like pigmentation in a family.

K Sandhu1, A Saraswat, A J Kanwar.   

Abstract

Dowling-Degos disease is a rare autosomal dominant inherited pigmentary disorder characterized by reticulate pigmentation of the flexures, prominent comedone like lesions and pitted scars. Dyschromatosis universalis hereditaria is characterized by the presence of hypopigmented as well as hyperpigmented macules. We report a family showing features of both these diseases.

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Year:  2004        PMID： 15482301     DOI： 10.1111/j.1468-3083.2004.01028.x

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


  4 in total

1.  Generalized dowling-degos disease: case reports.

Authors:  Jade Wititsuwannakul; Nopadon Noppakun
Journal:  Ann Dermatol       Date:  2013-08-13       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.  Atypical cases of Dowling-Degos disease.

Authors:  Kikkeri Narayanshetty Naveen; Sharatchandra B Athaniker; Spandana P Hegde; Rahul Shetty; Hanumanthayya Radha; Sadashivappa Sangam Parinitha
Journal:  Indian Dermatol Online J       Date:  2016 Mar-Apr

4.  Dermatoscopic Features of Hyper and Hypopigmented Lesions of Dowling Degos Disease.

Authors:  Balakrishnan Nirmal; Atul M Dongre; Uday S Khopkar
Journal:  Indian J Dermatol       Date:  2016 Jan-Feb       Impact factor: 1.494
  4 in total

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