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An instance of epidermal appendage anomaly that is caused by a modification of the individual's genome.
No clinical trials have been registered for hereditary epidermal appendage anomaly.
5 publications have been identified in PubMed for hereditary epidermal appendage anomaly. Research spans Review / Meta-Analysis (40%), Case Report / Case Series (40%), and Basic Science / Preclinical (20%).
Senapati B (2026). [PMID: 41075928](https://pubmed.ncbi.nlm.nih.gov/41075928/). *J Invest Dermatol*. [Basic Science / Preclinical]
Martínez-García JJ (2026). [PMID: 42166395](https://pubmed.ncbi.nlm.nih.gov/42166395/). *Am J Case Rep*. [Case Report / Case Series]
Paller AS (2025). [PMID: 40184496](https://pubmed.ncbi.nlm.nih.gov/40184496/). *Br J Dermatol*. [Review / Meta-Analysis]
Shimomura Y (2025). [PMID: 37407443](https://pubmed.ncbi.nlm.nih.gov/37407443/). *Keio J Med*. [Review / Meta-Analysis]
Mishra E (2024). [PMID: 39669041](https://pubmed.ncbi.nlm.nih.gov/39669041/). *J Orthop Case Rep*. [Case Report / Case Series]
Data assembled from 3 of 12 sources · Last updated Sep 18, 2026, 11:49 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center