Kisho is an information platform, not a medical provider. Nothing on this site constitutes medical advice, diagnosis, or treatment recommendations. All content is aggregated from publicly available sources (including ClinicalTrials.gov, PubMed, FDA.gov, and Orphanet) and is provided for informational purposes only. Clinical trial eligibility, treatment decisions, and any health-related actions should always be discussed with a qualified healthcare professional. Kisho does not endorse any specific therapy, organization, or clinical trial. Terms of use · Privacy policy
Features include: Hyperkeratosis lenticularis perstans.
Organ System | Phenotype Count | Example Features |
|---|---|---|
Skin | 1 | Hyperkeratosis lenticularis perstans |
Estimated prevalence: Unknown (Unknown prevalence).
No clinical trials have been registered for hyperkeratosis lenticularis perstans.
6 publications have been identified in PubMed for hyperkeratosis lenticularis perstans. Research spans Review / Meta-Analysis (50%) and Case Report / Case Series (50%).
Alaseeri KM (2025). [PMID: 41458780](https://pubmed.ncbi.nlm.nih.gov/41458780/). *Cureus*. [Case Report / Case Series]
Almatroud L (2025). [PMID: 40398887](https://pubmed.ncbi.nlm.nih.gov/40398887/). *Clinical and experimental dermatology*. [Review / Meta-Analysis]
Delrosso CA (2025). [PMID: 40103682](https://pubmed.ncbi.nlm.nih.gov/40103682/). *JAAD case reports*. [Case Report / Case Series]
Almatroud L (2025). [PMID: 40380040](https://pubmed.ncbi.nlm.nih.gov/40380040/). *Archives of dermatological research*. [Review / Meta-Analysis]
Mahmud MM (2025). [PMID: 39739501](https://pubmed.ncbi.nlm.nih.gov/39739501/). *Mymensingh medical journal : MMJ*. [Review / Meta-Analysis]
Data assembled from 5 of 12 sources · Last updated Oct 3, 2026, 8:11 PM UTC
Online Mendelian Inheritance in Man
European rare disease database
Genetic and Rare Diseases Info Center