Familial progressive hyper- and hypopigmentation (Q98797): Difference between revisions
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| Property / Canonical URI: https://id.who.int/icd/entity/1229773662 / rank | |||||||||||||||
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CID11:ID_1229773662 | |||||||||||||||
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dki-india-ID_1229773662 | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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15 August 2026
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Latest revision as of 15:24, 16 August 2026
Familial progressive hyper- and hypopigmentation is an autosomal dominant disorder of skin pigmentation characterised by progressive diffuse blotchy hypermelanosis accompanied by multiple café-au-lait macules, hypomelanotic macules and lentigines. It is thought to be due to mutations in the KIT ligand gene, mutations of which are also implicated in hereditary universal dyschromatosis.
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| default for all languages | ID_1229773662 |
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| English | Familial progressive hyper- and hypopigmentation |
Familial progressive hyper- and hypopigmentation is an autosomal dominant disorder of skin pigmentation characterised by progressive diffuse blotchy hypermelanosis accompanied by multiple café-au-lait macules, hypomelanotic macules and lentigines. It is thought to be due to mutations in the KIT ligand gene, mutations of which are also implicated in hereditary universal dyschromatosis. |
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CID11:ID_1229773662
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dki-india-ID_1229773662
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Concluído
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15 August 2026
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