Literature DB >> 2187721

Familial lichen planus.

V Katzenelson1, M Lotem, M Sandbank.   

Abstract

Familial lichen planus (FLP) was observed to have developed within a period of 3 years in 2 sisters as well as in the son of one of the women. In contrast to typical FLP, the eruption was generalized in only 1 of these patients; no atypical forms were observed; the response to topical treatment with steroids was rapid, and the relapses were few and mild. Previous reports of familial cases of lichen planus as well as the long interval between onset of the disease in the affected members of the family speak in favor of a genetic predisposition. HLA typing revealed HLA DR in all 3 patients. There was no increased incidence of HLA B7, HLA A3 or HLA A28.

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Year:  1990        PMID: 2187721     DOI: 10.1159/000248021

Source DB:  PubMed          Journal:  Dermatologica        ISSN: 0011-9075


  2 in total

1.  A retrospective and comparative study of familial and non-familial bullous lichen planus.

Authors:  Changzheng Huang; Xiaofeng Yan; Lingyun Yang; Jing Zhang; Jin Tian; Jiawen Li; Chunsen Wang; Yating Tu
Journal:  J Huazhong Univ Sci Technolog Med Sci       Date:  2007-06

2.  Familial Graham-Little-Picardi-Lassueur syndrome across 3 generations.

Authors:  Diego Soto-García; Carlos Feal-Cortizas; Carlos Álvarez; Carmen Couselo-Rodríguez; Sandra Martínez-Fernández; Ángeles Flórez
Journal:  JAAD Case Rep       Date:  2022-04-01
  2 in total

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