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Primary essential cutis verticis gyrata is a rare, progressive dermis disorder characterized by thickening of the scalp resulting in redundancy of the skin which gives rise to folds and grooves that give the scalp a cerebriform appearance. Folds cannot be corrected by pressure or traction and typically are symmetric and extend anteroposteriorly from vertex to occiput and/or transversely in occipital region. Additional features may include mild subungual hyperkeratosis and distal onycholysis of the nail plates of the great toes. It is not associated with neurological and ophthalmological changes, nor with secondary causes.
Estimated prevalence: Unknown (Unknown prevalence).
No clinical trials have been registered for primary essential cutis verticis gyrata.
1 publication has been identified in PubMed for primary essential cutis verticis gyrata. Research spans Case Report / Case Series (100%).
Oberoi V (2024). [PMID: 39439635](https://pubmed.ncbi.nlm.nih.gov/39439635/). *Cureus*. [Case Report / Case Series]
Data assembled from 3 of 12 sources · Last updated Sep 20, 2026, 3:05 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center