Fleshing out filaggrin phenotypes
- PMID: 17299430
- DOI: 10.1038/sj.jid.5700695
Fleshing out filaggrin phenotypes
Abstract
The association of filaggrin null alleles with eczema has been replicated in several European populations. Three large, well-conducted studies confirm this association and offer insights into the phenotypic nature of eczema associated with these alleles. Early data suggest that FLG-associated eczema may be more persistent, more likely to have palmar hyperlinearity, and more likely to be associated with asthma. These initial hints will require further confirmation in cohort studies.
Comment on
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Null mutations in the filaggrin gene (FLG) determine major susceptibility to early-onset atopic dermatitis that persists into adulthood.J Invest Dermatol. 2007 Mar;127(3):564-7. doi: 10.1038/sj.jid.5700587. Epub 2006 Sep 21. J Invest Dermatol. 2007. PMID: 16990802
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Two common loss-of-function mutations within the filaggrin gene predispose for early onset of atopic dermatitis.J Invest Dermatol. 2007 Mar;127(3):722-4. doi: 10.1038/sj.jid.5700579. Epub 2006 Sep 28. J Invest Dermatol. 2007. PMID: 17008875 No abstract available.
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Filaggrin mutations strongly predispose to early-onset and extrinsic atopic dermatitis.J Invest Dermatol. 2007 Mar;127(3):724-6. doi: 10.1038/sj.jid.5700630. Epub 2006 Nov 9. J Invest Dermatol. 2007. PMID: 17096018 No abstract available.
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