Flegel disease (Q105234): Difference between revisions
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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. |
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CID11:ID_932302493
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dki-india-ID_932302493
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