Acrogeria

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.

Also known as: Gottron Syndrome, Gottron syndrome, acrogeria, Gottron type, acrometageria, Metageria, familial acrogeria

0 clinical trials for this condition and its sub-types, 0 tagged with Acrogeria itself.