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Type 1 Segmental Galli-Galli Disease Resulting from a Previously Unreported Keratin 5 Mutation

  • Published:2012-08 Issue:8 Volume:132 Page:2100-2103
  • ISSN:0022-202X
  • Container-title:Journal of Investigative Dermatology
  • language:en
  • Short-container-title:Journal of Investigative Dermatology

Author:

Arnold Andreas W.,Kiritsi Dimitra,Happle Rudolf,Kohlhase Jürgen,Hausser Ingrid,Bruckner-Tuderman Leena,Has Cristina,Itin Peter H.

Publisher

Elsevier BV

Subject

Cell Biology,Dermatology,Molecular Biology,Biochemistry

Reference17 articles.

1. Dowling-Degos disease with asymmetrical axillary distribution and no KRT 5 exon 1 mutation;Asahina;Acta Derm Venereol,2007

2. Genodermatosis in a pair of brothers: Dowling-Degos, Grover, Darier, Hailey-Hailey or Galli-Galli disease?;Bardach;Hautarzt,1982

3. Loss-of-function mutations in the keratin 5 gene lead to Dowling-Degos disease;Betz;Am J Hum Genet,2006

4. Galli-Galli disease: an unrecognized entity or an acantholytic variant of Dowling-Degos disease?;Braun-Falco;J Am Acad Dermatol,2001

5. The genetic basis of Weber-Cockayne epidermolysis bullosa simplex;Chan;Proc Natl Acad Sci USA,1993

Cited by 11 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Galli–Galli Disease: A Comprehensive Literature Review;Dermatopathology;2024-02-07

2. Mosaic Manifestation of Autosomal Dominant Skin Disorders;Mosaicism in Human Skin;2022-11-24

3. Vielfältige Klinik, differenzierte Therapie;Deutsche Dermatologie;2022-10

4. Atypical Disseminated Variant of Galli–Galli Disease: A Review of the Literature;The American Journal of Dermatopathology;2020-07

5. Updated review of genetic reticulate pigmentary disorders;British Journal of Dermatology;2017-09-27
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