Flegel disease (Q105234): Difference between revisions

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Latest revision as of 11:18, 17 August 2026

Flegel disease is an inherited autosomal dominant disorder and is characterised by the development in early adult life of a profusion of 2–3 mm diameter keratotic papules with discrete irregular margins over the calves and the extensor surfaces of the ankles. Irritation may be severe and response to any form of treatment is poor.

Language	Label	Description	Also known as
default for all languages	ID_932302493
English	Flegel disease	Flegel disease is an inherited autosomal dominant disorder and is characterised by the development in early adult life of a profusion of 2–3 mm diameter keratotic papules with discrete irregular margins over the calves and the extensor surfaces of the ankles. Irritation may be severe and response to any form of treatment is poor.