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A congenital skin condition characterized by premature aging, more especially in the form of unusually fragile, thin skin on the hands and feet. Its onset is in early childhood; it progresses over the next few years and then remains stable. A bruising tendency has been observed.
Estimated prevalence: <1 in 1,000,000 (VERY_RARE).
No clinical trials have been registered for acrogeria.
1 publication has been identified in PubMed for acrogeria. Research spans Epidemiology / Natural History (100%).
Demirdas S (2024). [PMID: 38623759](https://pubmed.ncbi.nlm.nih.gov/38623759/). *Circulation. Genomic and precision medicine*. [Epidemiology / Natural History]
Data assembled from 4 of 12 sources · Last updated Sep 18, 2026, 3:23 PM UTC
Online Mendelian Inheritance in Man
European rare disease database
Genetic and Rare Diseases Info Center
Common questions about acrogeria