Abstract
We have recently shown that loss-of-function mutations in the filaggrin gene, carried by about 10% of people of European ethnicity, cause ichthyosis vulgaris and are strong predisposing factors for atopic dermatitis and asthma secondary to atopic dermatitis. These results demonstrate a prominent role for the epidermal barrier in atopic disease and have important implications for the study of complex traits.
MeSH terms
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Child
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Dermatitis, Atopic / genetics*
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Dermatitis, Atopic / metabolism
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Filaggrin Proteins
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Genes / genetics
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Genetic Predisposition to Disease*
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Humans
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Intermediate Filament Proteins / analysis
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Intermediate Filament Proteins / deficiency*
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Intermediate Filament Proteins / genetics*
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Mutation
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Skin / chemistry
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Skin / metabolism*
Substances
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FLG protein, human
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Filaggrin Proteins
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Intermediate Filament Proteins