Hereditary sclerosing poikiloderma, Weary type (Q101660): Difference between revisions
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As características cardinais desta rara condição autossômica dominante são poiquilodermia generalizada com acentuação em regiões flexurais, esclerose de palmas e plantas, hiperqueratose linear e bandas escleróticas nas axilas e fossas antecubitais e poplíteas, baquetamento digital. Pode ocorrer calcinose tecidual [OMIM]. | |||
| description / en | description / en | ||
The cardinal features of this rare autosomal dominant condition are generalised poikiloderma with accentuation in flexural regions, sclerosis of palms and soles, linear hyperkeratosis and sclerotic bands in the axillae and antecubital and popliteal fossae, clubbing of the fingers. Tissue calcinosis may occur [OMIM]. | |||
Revision as of 18:29, 16 August 2026
The cardinal features of this rare autosomal dominant condition are generalised poikiloderma with accentuation in flexural regions, sclerosis of palms and soles, linear hyperkeratosis and sclerotic bands in the axillae and antecubital and popliteal fossae, clubbing of the fingers. Tissue calcinosis may occur [OMIM].
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1538273632 |
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| English | Hereditary sclerosing poikiloderma, Weary type |
The cardinal features of this rare autosomal dominant condition are generalised poikiloderma with accentuation in flexural regions, sclerosis of palms and soles, linear hyperkeratosis and sclerotic bands in the axillae and antecubital and popliteal fossae, clubbing of the fingers. Tissue calcinosis may occur [OMIM]. |
