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Alopecia Areata Registry

Discussion in 'Women's Alopecia Areata' started by Joann, Aug 14, 2006.

  1. Joann

    Joann Moderator

    Mar 25, 2005
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    Hi Girls, :)

    I just wanted to put this up for all of you living in the U.S. and diagnosed with Alopecia Areata. NAAF urges everyone to take part in the Registry:

    " The Registry is a powerful tool to shine a light into furure research of alopecia areata. The data being gathered is being analyzed and will uncover clues to this mysterious disease"

    They are especially interested in:

    CONTROL SUBJECTS: people who don't have alopecia areata and aren't blood related to anyone who does

    MULIPLEX FAMILIES: three or more family or extended family members have been diagnosed with some form of alopecia areata

    SIBLING PAIRS: two or more siblings diagnosed with some form of alopecia areata

    TWINS: Either one or booth twin(s) diagnosed with alopecia areata

    Informative web site: http://www.AlopeciaAreataRegistry.org

    Phone number: 1-866-837-1050

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