Rare Lichen Planus

Watchlist

(log in to enable)

Retrieved

2022-04-26

Source

Gard

Trials

—

Genes

IFNG, TNF, IL6, BCL2, FOXP3, DSG1, ERVW-1, IL23A, JAK1, HLA-DRB1, CXCR3, CXCL9, FLG, DSG3, IL17A, PTGS2, VCAM1, VIM, ABCC8, YME1L1, ZEB1, TGFB1, GNLY, ABCB6, TGM2, TLR4, APOBEC3B, AIM2, NRP2, TP63

IFNG, TNF, IL6, BCL2, FOXP3, DSG1, ERVW-1, IL23A, JAK1, HLA-DRB1, CXCR3, CXCL9, FLG, DSG3, IL17A, PTGS2, VCAM1, VIM, ABCC8, YME1L1, ZEB1, TGFB1, GNLY, ABCB6, TGM2, TLR4, APOBEC3B, AIM2, NRP2, TP63, TP53, TWIST1, UVRAG, CKAP4, WNT5A, ADM, VASH1, MIR155HG, LINC02210-CRHR1, MIR31, MIR203A, MIR155, IL31, CLEC4C, RBM45, TCHHL1, DCD, NLRP3, SERPINB4, TSLP, ABCC11, HAVCR2, HOPX, PDCD1LG2, WLS, MARCKSL1, CARD18, DUOX1, STAT1, PRL, S100A9, CRHR1, ICAM1, HMGB1, HLA-DQA1, HLA-A, GZMB, GPT, FLT4, ERBB2, ELANE, CRH, S100A8, CLDN7, COL17A1, CHI3L1, CDA, CASP3, CASP1, CAMP, C5AR1, APOB, IFNA1, IFNA13, IFNB1, IGFBP4, RPE65, MOK, AGER, PECAM1, PDC, MTHFR, COX2, ABCC1, MMP9, MMP3, MMP2, LTA, LCN2, LAMP1, JAK2, IVL, ITGB2, IRF7, IDO1, MTCO2P12

Drugs

—

Interested in hearing about new therapies?

Rare lichen planus (rare LP) refers to several rare variants of lichen planus, which is a condition that affects the skin and/or mouth. The signs and symptoms vary by subtype but generally include an itchy rash. In most cases, the exact underlying cause of rare LP is unknown; however, studies suggest that it may be due to an allergic or immune reaction. Treatment is based on the signs and symptoms present in each person; however, intervention is not always necessary as some cases of rare LP resolve on their own.