Abstract
Acrokeratoelastoidosis (AKE) is a genodermatosis characterized by small, firm papules or plaques on the sides of the hands and feet 1, it was first described in 1953 by Costa, in a Brazilian patient. It is a rare disease, both autosomal dominant and sporadic forms have been observed 2. It is characterized by multiple hyperkeratotic papules on the palms, soles, and dorsum of the hands and feet.
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