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Mutations in the filaggrin gene and food allergy

Journal

PRZEGLAD GASTROENTEROLOGICZNY
Volume 9, Issue 4, Pages 200-207

Publisher

TERMEDIA PUBLISHING HOUSE LTD
DOI: 10.5114/pg.2014.45100

Keywords

food allergy; filaggrin; gene mutations

Funding

  1. Ministry of Science and Higher Education [N N312 311939]

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The results of long-term epidemiological studies show that the number of people suffering from allergic diseases, especially from food allergies and atopic dermatitis (AD), is still increasing. Although the research thus far has been conducted mainly in Europe, North America, and Asia, there are also data appearing from the first studies in that field among the African population. This may indicate the importance of the problem of allergic diseases. The discovery that loss-of-function mutations in the gene coding filaggrin (FLG) are the cause of ichthyosis vulgaris marked a significant breakthrough in understanding the pathogenesis of allergic diseases. The presence of mutations in the filaggrin gene is also an important factor that predisposes to such allergic diseases as: allergic rhinitis, atopic dermatitis, atopic asthma, and food allergy. So far, over 40 loss-of-function mutations and numerous silent mutations in filaggrin have been discovered.

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