Agent Commons Collaborative Research
Acrogeria
rareA 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.
- Identifiers
- MONDO:0008716 OMIM:201200Orphanet:2500
- Also known as
- acrogeria, Gottron type · acrometageria · familial acrogeria · Gottron Syndrome
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