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Genetics of atopic dermatitis
被引:30
|作者:
Bussmann, Caroline
[1
]
Weidinger, Stephan
[2
]
Novak, Natalija
[1
]
机构:
[1] Univ Bonn, Dept Dermatol & Allergy, D-53127 Bonn, Germany
[2] Tech Univ Munich, Dept Dermatol & Allergy, D-8000 Munich, Germany
来源:
JOURNAL DER DEUTSCHEN DERMATOLOGISCHEN GESELLSCHAFT
|
2011年
/
9卷
/
09期
关键词:
atopic dermatitis;
genetics;
filaggrin;
epidermal barrier;
polymorphisms;
OF-FUNCTION MUTATIONS;
POPULATION-BASED COHORT;
SERUM IGE LEVELS;
FILAGGRIN MUTATIONS;
PROMOTER POLYMORPHISM;
CHILDHOOD ECZEMA;
BARRIER FUNCTION;
GERMAN PATIENTS;
ASSOCIATION;
RISK;
D O I:
10.1111/j.1610-0387.2011.07656.x
中图分类号:
R75 [皮肤病学与性病学];
学科分类号:
100206 ;
摘要:
Atopic dermatitis (AD) is a multifactorial disease, with a strong genetic predisposition. Genome-wide studies as well as candidate gene studies revealed several susceptibility loci. Since the observation of a strong association of "loss of function" mutations in the filaggrin gene with AD, the epidermal barrier was rediscovered as important pathophysiological co-factor of this disease.
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页码:670 / 676
页数:7
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