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Autosomal dominant form of hypohidrotic ectodermal dysplasia.
Estimated prevalence: <1 in 1,000,000 (VERY_RARE).
No clinical trials have been registered for autosomal dominant hypohidrotic ectodermal dysplasia.
3 publications have been identified in PubMed for autosomal dominant hypohidrotic ectodermal dysplasia. Research spans Case Report / Case Series (67%) and Epidemiology / Natural History (33%).
Kovalskaia VA (2026). [PMID: 41645317](https://pubmed.ncbi.nlm.nih.gov/41645317/). *Orphanet J Rare Dis*. [Epidemiology / Natural History]
Mukhtar MA (2025). [PMID: 42232673](https://pubmed.ncbi.nlm.nih.gov/42232673/). *Pan Afr Med J*. [Case Report / Case Series]
Reddy H (2024). [PMID: 38854244](https://pubmed.ncbi.nlm.nih.gov/38854244/). *Cureus*. [Case Report / Case Series]
Data assembled from 3 of 12 sources · Last updated Sep 20, 2026, 6:50 AM UTC
European rare disease database
Genetic and Rare Diseases Info Center