A prospective study of filaggrin null mutations in keratoconus patients with or without atopic disorders.

Droitcourt, C; Touboul, D; Ged, C; Ezzedine, K; Cario-André, M; de Verneuil, H; Colin, J; Taïeb, A

Droitcourt, C; Touboul, D; Ged, C; Ezzedine, K; Cario-André, M; de Verneuil, H; Colin, J; Taïeb, A.

Affiliation

Droitcourt C; Department of Dermatology, National Reference Centre for Rare Skin Disorders, CHU de Bordeaux, Bordeaux, France. catherine.droitcourt@gmail.com

Dermatology ; 222(4): 336-41, 2011.

Article in En | MEDLINE | ID: mdl-21701148

Subject(s)

Dermatitis, Atopic/genetics; Intermediate Filament Proteins/genetics; Keratoconus/genetics; Mutation; Adolescent; Adult; Child; Dermatitis, Atopic/epidemiology; Female; Filaggrin Proteins; Genetic Predisposition to Disease/epidemiology; Humans; Keratoconus/epidemiology; Male; Middle Aged; Prevalence; Prospective Studies; Young Adult

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Dermatitis, Atopic / Intermediate Filament Proteins / Keratoconus / Mutation Type of study: Observational_studies / Prevalence_studies / Risk_factors_studies Limits: Adolescent / Adult / Child / Female / Humans / Male / Middle aged Language: En Journal: Dermatology Journal subject: DERMATOLOGIA Year: 2011 Type: Article Affiliation country: France

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