Familial progressive hyper- and hypopigmentation (Q98797)
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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.
| Language | Label | Description | Also known as |
|---|---|---|---|
| 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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