Diffuse epidermolytic palmoplantar keratoderma (Q85670): Difference between revisions
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A ceratodermia palmoplantar epidermolítica difusa de Vörner-Thost (MIM #144200) é um transtorno autossômico dominante que é clinicamente indistinguível da ceratodermia palmoplantar não epidermolítica difusa (Unna), mas tem diferentes aparência histológica (hiperceratose epidermolítica) e etiologia (mutações de queratina 9). A ceratodermia difusa se desenvolve na infância, levando à ceratodermia confluente, poupando superfícies dorsais, com demarcação nítida e borda eritematosa na vida adulta. | |||
| description / en | description / en | ||
Diffuse epidermolytic palmoplantar keratoderma of Vörner-Thost (MIM #144200) is an autosomal dominant disorder which is clinically indistinguishable from diffuse non-epidermolytic palmoplantar keratoderma (Unna) but has different histological appearance (epidermolytic hyperkeratosis) and aetiology (keratin 9 mutations). Diffuse keratoderma develops in infancy, leading to confluent keratoderma, sparing dorsal surfaces, with a sharp demarcation and erythematous edge by adult life. | |||
Revision as of 11:02, 15 August 2026
Diffuse epidermolytic palmoplantar keratoderma of Vörner-Thost (MIM #144200) is an autosomal dominant disorder which is clinically indistinguishable from diffuse non-epidermolytic palmoplantar keratoderma (Unna) but has different histological appearance (epidermolytic hyperkeratosis) and aetiology (keratin 9 mutations). Diffuse keratoderma develops in infancy, leading to confluent keratoderma, sparing dorsal surfaces, with a sharp demarcation and erythematous edge by adult life.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1505856808 |
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| English | Diffuse epidermolytic palmoplantar keratoderma |
Diffuse epidermolytic palmoplantar keratoderma of Vörner-Thost (MIM #144200) is an autosomal dominant disorder which is clinically indistinguishable from diffuse non-epidermolytic palmoplantar keratoderma (Unna) but has different histological appearance (epidermolytic hyperkeratosis) and aetiology (keratin 9 mutations). Diffuse keratoderma develops in infancy, leading to confluent keratoderma, sparing dorsal surfaces, with a sharp demarcation and erythematous edge by adult life. |
