Steatocystoma multiplex with hair shaft abnormalities

Author:

Pietrzak Aldona1,Bartosinska Joanna1,Filip Agata A.2,Rakowska Adriana3,Adamczyk Michal1,Szumilo Justyna4,Kanitakis Jean5

Affiliation:

1. Department of Dermatology; Venereology and Pediatric Dermatology; Medical University of Lublin; Lublin Poland

2. Department of Cancer Genetics; Medical University of Lublin; Lublin Poland

3. Dermatology Department; CSK MSW; Warsaw Poland

4. Department of Clinical Pathomorphology; Medical University of Lublin; Lublin Poland

5. Department of Dermatology; Ed. Herriot Hospital Group; Lyon France

Publisher

Wiley

Subject

Dermatology,General Medicine

Reference15 articles.

1. Steatocystoma multiplex- a rare genetic disorder: a case report and review of the literature;Kamra;J Clin Diagn Res,2013

2. A novel missense mutation of keratin 17 gene in a Chinese family with steatocystoma multiplex;Ha;Ann Dermatol,2013

3. Steatocystoma multiplex, oligodontia and partial persistent primary dentition associated with a novel keratin 17 mutation;Gass;Br J Dermatol,2009

4. Steatocystoma multiplex: keratin 17 - the key player?;Antal;Br J Dermatol,2012

5. Localized forms of steatocystoma multiplex: case report and review of the literature;Mortazavi;Dermatol Online J,2005

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