Dup15q Alliance provides family support and promotes awareness, research and targeted treatments for chromosome 15q11.2-13.1 duplication syndrome.
Through our work to raise awareness and promote research into chromosome 15q duplications, we seek to find targeted treatments so that affected individuals can live full and productive lives. Together with our families, Dup15q Alliance is working towards a better tomorrow for children with chromosome 15q11.2-13.1 duplication (dup15q) syndrome.
The Mirror is published quarterly to educate families about duplications of chromosome 15q, share family stories, and provide information about treatment options and current research.
Dup15q Alliance matches parents seeking support with parent mentors who can provide emotional support.
Dup15q Alliance supports small regional meetings for families to network, share resources and support.
Dup15q Alliance family conferences are held every other year to provide families with an opportunity to meet and learn about scientific and treatment advances.
The Facebook online community brings together those affected by dup15q syndrome to share information, stories and ideas. Families and individuals with dup15q come from a wide range of backgrounds and are dealing with a variety of day-to-day issues. We are here to make friends, support each other and help do our best for the ones that we love.
The official Dup15q Alliance Facebook Page can be found at Dup15q Alliance. We also facilitate a parent-only Facebook page at Dup15q Alliance Parent Support Group.
The official Dup15q Alliance Twitter Page can be found @dup15q.
Dup15q Alliance works with researchers to connect our families with research opportunities and expand research into dup15q syndrome
The Human Genetic Cell Repository at the Coriell Institute for Medical Research holds a collection of chromosome 15q duplication cell lines for use in research. Families are encouraged to donate cell lines to this collection.
Upon the death of an individual with chromosome 15q11.2-13.1 duplication syndrome, families are encouraged to consider donating brain and tissues of the deceased to the Autism Tissue Program to expand these vitally needed resources for research.