Oral lichen planus in a patient with neurofibromatosis type 1: a case report

IntroductionNeurofibromatosis type 1 (NF1) is one of the most common autosomal dominant genetic disorders, with an estimated prevalence of 1 in 2,500 to 3,000 individuals worldwide. It results from pathogenic variants in the NF1 gene on chromosome 17,

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Published
2025-10-10
DOI
https://doi.org/10.22541/au.176008697.74428885/v1
Primary Topic
Cancer Diagnosis and Treatment
Type
article
Field-Weighted Citation Impact
0.00

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article

Oral lichen planus in a patient with neurofibromatosis type 1: a case report

S A Mousavi, Mehdi Abrishami, Amirmansour shirani, Hamid Taherinya
Cancer Diagnosis and Treatment
article

Oral lichen planus in a patient with neurofibromatosis type 1: a case report

S A Mousavi, Mehdi Abrishami, Amirmansour shirani, Hamid Taherinya
article en

Abstract

IntroductionNeurofibromatosis type 1 (NF1) is one of the most common autosomal dominant genetic disorders, with an estimated prevalence of 1 in 2,500 to 3,000 individuals worldwide. It results from pathogenic variants in the NF1 gene on chromosome 17,

Islamic Azad University, Isfahan (IR), University of Isfahan (IR)
Islamic Azad University
Openalex Percentile: Top 61%
Cancer Diagnosis and Treatment
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Oral lichen planus in a patient with neurofibromatosis type 1: a case report — S A Mousavi, Mehdi Abrishami, et al. · (2025) | TGRS Research Map | TGRS