Alopecia Areata
Kerstin Foitzik-Lau
Skin and Vein Clinic Winterhude, Hamburg, Germany
Search for more papers by this authorKerstin Foitzik-Lau
Skin and Vein Clinic Winterhude, Hamburg, Germany
Search for more papers by this authorPeter Hoeger
Search for more papers by this authorVeronica Kinsler
Search for more papers by this authorAlbert Yan
Search for more papers by this authorJohn Harper
Search for more papers by this authorArnold Oranje
Search for more papers by this authorChristine Bodemer
Search for more papers by this authorMargarita Larralde
Search for more papers by this authorVibhu Mendiratta
Search for more papers by this authorDiana Purvis
Search for more papers by this authorSummary
Alopecia areata (AA) is an autoimmune disease with a genetic basis and environmental triggers. It presents as nonscarring hair loss ranging from few circular bald areas (patchy alopecia areata) to complete baldness of the head (alopecia totalis) or the entire body (alopecia universalis). Almost 2% of the population is affected once in a lifetime. The peak onset in childhood is before the age of 10. The genetic trait is complex and still not completely understood. Indeed, genome-wide association studies have given more insight into the pathogenesis of AA and opened new therapeutic options. It is now widely accepted that a collapse of the immune privilege of the hair follicle is responsible for AA activation which enables immune cells to attack the hair follicle. First studies using inhibitors of the JAK kinase pathway have shown promising results in the treatment of AA.
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