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An instance of hydroa vacciniforme that is caused by an inherited modification of the individual's genome.
No clinical trials have been registered for hydroa vacciniforme, familial.
3 publications have been identified in PubMed for hydroa vacciniforme, familial. Research spans Review / Meta-Analysis (100%).
Adya KA (2025). [PMID: 40709861](https://pubmed.ncbi.nlm.nih.gov/40709861/). *Indian Dermatol Online J*. [Review / Meta-Analysis]
Rukerd MRZ (2024). [PMID: 39497062](https://pubmed.ncbi.nlm.nih.gov/39497062/). *BMC Infect Dis*. [Review / Meta-Analysis]
Jin J (2024). [PMID: 38502913](https://pubmed.ncbi.nlm.nih.gov/38502913/). *Ann Med*. [Review / Meta-Analysis]
Data assembled from 3 of 12 sources · Last updated Sep 18, 2026, 7:15 PM UTC
Online Mendelian Inheritance in Man
Genetic and Rare Diseases Info Center
AI-curated news mentioning hydroa vacciniforme, familial
Updated Apr 24, 2026
A recent publication discusses the clinical features and diagnostic criteria for hydroa vacciniforme, a rare photosensitive condition. The article emphasizes the importance of early recognition and management to improve patient outcomes.