Acrogeria
MONDO:0008716A 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
7 clinical trials for this condition and its sub-types.
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Disease
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Hereditary disease
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Skin disorder
(123)
Human disease
(14)
Premature aging syndrome
(6)
Hereditary skin disorder
(5)
Disease of genetic or genomic mechanism
(2)
Disease by body system or component
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Disease by developmental or physiological process
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Disease by etiologic mechanism
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