Porokeratoses (Q44109): Difference between revisions
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As poroceratoses resultam de um transtorno clonal de queratinização. Elas são caracterizadas por uma ou mais placas atróficas circundadas por uma borda hiperceratótica estriada clínica e histologicamente distinta (lamela cornoide). Múltiplas variantes clínicas da poroceratose são reconhecidas. | |||
| description / en | description / en | ||
Porokeratoses result from a clonal disorder of keratinization. They are characterised by one or more atrophic patches surrounded by a clinically and histologically distinctive ridged hyperkeratotic border (cornoid lamella). Multiple clinical variants of porokeratosis are recognised. | |||
Revision as of 11:26, 13 August 2026
Porokeratoses result from a clonal disorder of keratinization. They are characterised by one or more atrophic patches surrounded by a clinically and histologically distinctive ridged hyperkeratotic border (cornoid lamella). Multiple clinical variants of porokeratosis are recognised.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ED52 |
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| English | Porokeratoses |
Porokeratoses result from a clonal disorder of keratinization. They are characterised by one or more atrophic patches surrounded by a clinically and histologically distinctive ridged hyperkeratotic border (cornoid lamella). Multiple clinical variants of porokeratosis are recognised. |
