Keratosis follicularis spinulosa decalvans (Q95829): Difference between revisions
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Ceratose folicular espinhosa decalvante é uma genodermatose rara que ocorre durante a infância, acometendo predominantemente indivíduos do sexo masculino e caracterizada por hiperceratose folicular difusa associada à alopecia cicatricial progressiva de couro cabeludo, sobrancelhas e cílios. Achados adicionais podem incluir fotofobia, distrofia corneana, eritema facial e/ou ceratodermia palmoplantar. | |||
| description / en | description / en | ||
Keratosis follicularis spinulosa decalvans is a rare genodermatosis occurring during infancy or childhood, predominantly affecting males, and characterised by diffuse follicular hyperkeratosis associated with progressive cicatricial alopecia of the scalp, eyebrows and eyelashes. Additional findings can include photophobia, corneal dystrophy, facial erythema, and/or palmoplantar keratoderma. | |||
Revision as of 11:39, 16 August 2026
Keratosis follicularis spinulosa decalvans is a rare genodermatosis occurring during infancy or childhood, predominantly affecting males, and characterised by diffuse follicular hyperkeratosis associated with progressive cicatricial alopecia of the scalp, eyebrows and eyelashes. Additional findings can include photophobia, corneal dystrophy, facial erythema, and/or palmoplantar keratoderma.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_303213910 |
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| English | Keratosis follicularis spinulosa decalvans |
Keratosis follicularis spinulosa decalvans is a rare genodermatosis occurring during infancy or childhood, predominantly affecting males, and characterised by diffuse follicular hyperkeratosis associated with progressive cicatricial alopecia of the scalp, eyebrows and eyelashes. Additional findings can include photophobia, corneal dystrophy, facial erythema, and/or palmoplantar keratoderma. |
