Erythrokeratodermia variabilis et progressiva (Q94074): Difference between revisions

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A eritroqueratodermia variável do tipo Mendes da Costa (EKV) é uma genodermatose caracterizada pelo aparecimento de duas lesões cutâneas independentes: manchas eritematosas figuradas transitórias e hiperceratose que é geralmente localizada, mas ocasionalmente ocorre em sua forma generalizada, geralmente durante o primeiro ano de vida.
description / endescription / en
 
Mendes da Costa type erythrokeratodermia variabilis (EKV) is a genodermatosis characterised by the appearance of two independent skin lesions: transient figurate erythematous patches and hyperkeratosis that is usually localised but occasionally occurs in its generalised form, generally during the first year of life.
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Property / Canonical URI: https://id.who.int/icd/entity/886266813 / rank
 
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Property / CURIE
 
CID11:ID_886266813
Property / CURIE: CID11:ID_886266813 / rank
 
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Property / Canary Token
 
dki-india-ID_886266813
Property / Canary Token: dki-india-ID_886266813 / rank
 
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Concluído
Property / Verification Status: Concluído / rank
 
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Property / Knowledge Architect
 
Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
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15 August 2026
Timestamp+2026-08-15T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
Property / Collection date: 15 August 2026 / rank
 
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Latest revision as of 09:11, 16 August 2026

Mendes da Costa type erythrokeratodermia variabilis (EKV) is a genodermatosis characterised by the appearance of two independent skin lesions: transient figurate erythematous patches and hyperkeratosis that is usually localised but occasionally occurs in its generalised form, generally during the first year of life.
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ID_886266813
    English
    Erythrokeratodermia variabilis et progressiva
    Mendes da Costa type erythrokeratodermia variabilis (EKV) is a genodermatosis characterised by the appearance of two independent skin lesions: transient figurate erythematous patches and hyperkeratosis that is usually localised but occasionally occurs in its generalised form, generally during the first year of life.

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      CID11:ID_886266813
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      dki-india-ID_886266813
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      Concluído
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      15 August 2026
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