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

Diego Soto-García; Carlos Feal-Cortizas; Carlos Álvarez; Carmen Couselo-Rodríguez; Sandra Martínez-Fernández; Ángeles Flórez

doi:10.1016/j.jdcr.2022.03.033

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

JAAD Case Rep. 2022 Apr 1:23:128-132. doi: 10.1016/j.jdcr.2022.03.033. eCollection 2022 May.

Authors

Diego Soto-García^{1

2}, Carlos Feal-Cortizas^{1

2}, Carlos Álvarez^{1

3}, Carmen Couselo-Rodríguez^{1

2}, Sandra Martínez-Fernández^{1

2}, Ángeles Flórez^{1

2}

Affiliations

¹ Dermatología inflamatoria, pediátrica y oncológica Research Group, Galicia Sur Health Research Institute (Instituto Investigación Sanitaria Galicia Sur), SERGAS-UVIGO, Vigo, Spain.
² Department of Dermatology, University Hospital of Pontevedra, Pontevedra, Spain.
³ Department of Pathology, University Hospital of Pontevedra, Pontevedra, Spain.

No abstract available

Keywords: GLPLS, Graham-Little-Piccardi-Lassueur syndrome; HLA, human leukocyte antigen; LPP, lichen planopilaris; familial Graham-Little-Piccardi-Lassueur syndrome; lichen planopilaris; scarring alopecia.

Publication types

Case Reports