Flegel disease (Q105234): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed label, description and/or aliases in pt-br, en |
||
| description / pt-br | description / pt-br | ||
A doença de Flegel é um transtorno hereditário autossômico dominante e é caracterizada pelo desenvolvimento no início da vida adulta de uma profusão de pápulas ceratóticas de 2 a 3 mm de diâmetro com margens irregulares distintas sobre as panturrilhas e as superfícies extensoras dos tornozelos. A irritação pode ser grave e a resposta a qualquer forma de tratamento é insuficiente. | |||
| description / en | description / en | ||
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. | |||
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. |
