Keratosis pilaris (Q43778): Difference between revisions
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Ceratose pilar é uma anormalidade muito comum da queratinização caracterizada pelo tamponamento ceratótico dos orifícios foliculares com graus variados de eritema perifolicular. É observada em até metade das crianças normais e em três quartos das crianças com ictiose vulgar. Os lados da face e as superfícies extensoras dos braços são localizações de predileção. A herança autossômica dominante muitas vezes pode ser demonstrada. Em algumas variantes, a atrofia ou a pigmentação podem ser mais proeminentes do que a ceratose. | |||
| description / en | description / en | ||
Keratosis pilaris is a very common abnormality of keratinization characterised by keratinous plugging of follicular orifices with varying degrees of perifollicular erythema. It is seen in up to half of normal children and in three quarters of children with ichthyosis vulgaris. The sides of the face and the extensor surfaces of the upper arms are sites of predilection. Autosomal dominant inheritance can often be demonstrated. In some variants atrophy or pigmentation may be more prominent than keratosis. | |||
Revision as of 10:55, 13 August 2026
Keratosis pilaris is a very common abnormality of keratinization characterised by keratinous plugging of follicular orifices with varying degrees of perifollicular erythema. It is seen in up to half of normal children and in three quarters of children with ichthyosis vulgaris. The sides of the face and the extensor surfaces of the upper arms are sites of predilection. Autosomal dominant inheritance can often be demonstrated. In some variants atrophy or pigmentation may be more prominent than keratosis.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ED56 |
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| English | Keratosis pilaris |
Keratosis pilaris is a very common abnormality of keratinization characterised by keratinous plugging of follicular orifices with varying degrees of perifollicular erythema. It is seen in up to half of normal children and in three quarters of children with ichthyosis vulgaris. The sides of the face and the extensor surfaces of the upper arms are sites of predilection. Autosomal dominant inheritance can often be demonstrated. In some variants atrophy or pigmentation may be more prominent than keratosis. |
