Genetic basis of alopecia areata: a roadmap for translational research.

Abstract:

:Alopecia areata (AA) is a recurrent autoimmune type of hair loss that affects about 5.3 million people in the United States alone. Despite being the most prevalent autoimmune disease, the molecular and cellular mechanisms underlying this complex disease are still poorly understood, and rational treatments are lacking. Further efforts are necessary to clearly pinpoint the causes and molecular pathways leading to this disease and to find evidence-based treatments for AA. The authors focus on the central role of genetics for gaining insight into disease pathogenesis and setting the stage for the rational development of novel effective therapeutic approaches.

journal_name

Dermatol Clin

journal_title

Dermatologic clinics

authors

Jabbari A,Petukhova L,Cabral RM,Clynes R,Christiano AM

doi

10.1016/j.det.2012.08.014

subject

Has Abstract

pub_date

2013-01-01 00:00:00

pages

109-17

issue

1

eissn

0733-8635

issn

1558-0520

pii

S0733-8635(12)00102-7

journal_volume

31

pub_type

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