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White sponge nevus (WSN) is a rare and autosomal dominant genetic disease in which the oral mucosa is white or grayish, thickened, folded, and spongy. The onset is early in life, and both sexes are affected equally. Other common sites include the tongue, floor of the mouth, and alveolar mucosa.
No clinical trials have been registered for hereditary mucosal leukokeratosis.
6 publications have been identified in PubMed for hereditary mucosal leukokeratosis. Research spans Case Report / Case Series (100%).
Hosseinpour Sarmadi M (2025). [PMID: 40893399](https://pubmed.ncbi.nlm.nih.gov/40893399/). *Clinical case reports*. [Case Report / Case Series]
Prada-García C (2024). [PMID: 38594177](https://pubmed.ncbi.nlm.nih.gov/38594177/). *Anais brasileiros de dermatologia*. [Case Report / Case Series]
Llull-Ramos A (2024). [PMID: 39102980](https://pubmed.ncbi.nlm.nih.gov/39102980/). *Actas dermo-sifiliograficas*. [Case Report / Case Series]
Spodzieja K (2024). [PMID: 39563015](https://pubmed.ncbi.nlm.nih.gov/39563015/). *The American journal of case reports*. [Case Report / Case Series]
Spodzieja K (2024). [PMID: 39704005](https://pubmed.ncbi.nlm.nih.gov/39704005/). *The American journal of case reports*. [Case Report / Case Series]
Data assembled from 3 of 12 sources · Last updated Sep 18, 2026, 11:37 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center