Oral mucosal lesions in xeroderma pigmentosum type C in Mayotte

Clicks: 2
ID: 318228
2026
Free PDF
Article Quality & Performance Metrics
Overall Quality
Not rated
Combines reader engagement with the AI quality analysis. This article has not been analysed, so there is no overall score — reader engagement is measured and shown alongside.
AI Quality Assessment
Not analyzed
Readership in this journal
Emerging

Ranked #241 of 304 articles by views in the british journal of dermatology

Most read Least read

Bar heights use a square-root scale. Only the 120 most-read articles are drawn; the journal has 304 in total.

Mint this article as an NFT
Not yet minted

Create a permanent, verifiable on-chain record of this article on the Scimatic Network. The NFT is held in your Journament account, and you can withdraw it to your own wallet at any time.

5 SUSD one-off · no wallet required
Sign in to mint
Abstract
Xeroderma Pigmentosum (XP) is a rare autosomal recessive disorder caused by defective DNA repair, leading to a high cancer risk. While skin and eye symptoms are well known, oral involvement is less studied. In a retrospective study of 23 XP-C patients from Mayotte sharing the same mutation, oral lesions - especially on the lips and tongue - were frequent and appeared early. All patients showed tongue abnormalities by age 12, including precancerous lesions and carcinomas. These findings reveal a distinct, early-onset pattern and stress the need for systematic oral monitoring.
Reference Key
openalex_W7165563511 Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Marc Dumas, Antoine Willemart, Nolwenn Lepouriel, Alice Miquel, S. Hadj‐Rabia, Antoine Bertolotti
Journal the british journal of dermatology
Year 2026
DOI
10.1093/bjd/ljag252
URL
https://doi.org/10.1093/bjd/ljag252
Keywords Keywords not found

Citations

No citations found. To add a citation, contact the admin at info@scimatic.org

Comments

No comments yet. Be the first to comment on this article.