Lichen planopilaris in three generations: grandmother, mother, and daughter - a genetic link?
Author:
Affiliation:
1. Department of Dermatology; Medical University of Warsaw; Warsaw Poland
Publisher
Wiley
Subject
Dermatology
Reference6 articles.
1. Lichen planopilaris is associated with HLA DRB1*11 and DQB1*03 alleles;Pavlovsky;Acta Derm Venereol,2015
2. Trichoscopy of cicatricial alopecia;Rakowska;J Drugs Dermatol,2012
3. Familial Lassueur-Graham-Little-Piccardi syndrome;Viglizzo;Dermatology,2004
4. Gsdma3 mutation causes bulge stem cell depletion and alopecia mediated by skin inflammation;Zhou;Am J Pathol,2012
5. Lichen planopilaris and pseudopelade of Brocq involve distinct disease associated gene expression patterns by microarray;Yu;J Dermatol Sci,2010
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1. Frontiers in Lichen Planopilaris and Frontal Fibrosing Alopecia Research: Pathobiology Progress and Translational Horizons;JID Innovations;2022-05
2. Graham‐Little‐Piccardi‐Lassueur syndrome in siblings;International Journal of Dermatology;2021-03-27
3. Frontal fibrosing alopecia: An update on the hypothesis of pathogenesis and treatment;International Journal of Women's Dermatology;2019-06
4. Lichen Planopilaris;Alopecia;2019
5. Lichen planopilaris with Koebner phenomenon;JAAD Case Reports;2018-09
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