Xeroderma pigmentosum G (Q92842): Difference between revisions
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Revision as of 07:57, 16 August 2026
Xeroderma pigmentosum complementation group G (XPG) is an extremely rare subtype of xeroderma pigmentosum (XP), a rare photodermatosis predisposing to skin cancers. Clinical manifestations can vary as some patients present with a mild XP phenotype (UV sensitivity, hyper- or hypo-pigmented skin lesions and increased incidence of skin cancer) and others combine symptoms of XP with systemic and neurological manifestations of Cockayne syndrome (XP/CS complex).
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_2086751990 |
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| English | Xeroderma pigmentosum G |
Xeroderma pigmentosum complementation group G (XPG) is an extremely rare subtype of xeroderma pigmentosum (XP), a rare photodermatosis predisposing to skin cancers. Clinical manifestations can vary as some patients present with a mild XP phenotype (UV sensitivity, hyper- or hypo-pigmented skin lesions and increased incidence of skin cancer) and others combine symptoms of XP with systemic and neurological manifestations of Cockayne syndrome (XP/CS complex). |
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CID11:ID_2086751990
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dki-india-ID_2086751990
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Concluído
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