Hereditary sclerosing poikiloderma, Weary type (Q101660): Difference between revisions
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dki-india-ID_1538273632 | |||||||||||||||
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15 August 2026
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Latest 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 |
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| 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]. |
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CID11:ID_1538273632
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dki-india-ID_1538273632
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Concluído
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15 August 2026
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