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Call for Participation: Identical Twins Needed for Groundbreaking 22q11 Research

„Same DNA, Different Outcomes – Help Us Unravel the Mystery!”

Dear 22q11 Associations and Advocates Worldwide,

We are reaching out to you with an exciting opportunity to contribute to vital research on 22q11 deletion and duplication syndrome. Dr. Beata Nowakowska, a renowned geneticist specializing in 22q11, and her research team are conducting an in-depth study to better understand the molecular mechanisms underlying the syndrome. They are currently seeking identical (monozygotic) twins diagnosed with 22q11 deletion or duplication to participate in this groundbreaking study.

Why Identical Twins?

Identical twins share the same DNA, yet they often present with different symptoms (phenotypic differences). This intriguing variation provides a unique opportunity to explore how genetic and epigenetic factors influence the syndrome. The study will focus on:

• DNA methylation patterns

• Genomic and transcriptomic profiling

• Molecular differences between twins

Who Can Participate?

We are looking for identical (monozygotic) twins with:

• A confirmed diagnosis of 22q11 deletion or duplication (or willingness to undergo confirmation)

• Willingness to contribute a small blood sample

• Participants from any country

How Can You Help?

We kindly ask for your assistance in sharing this announcement with your networks, local support groups, and families affected by 22q11 worldwide. Your help in spreading the word could significantly advance our understanding of 22q11-related conditions and lead to improved treatments in the future.

For further details or to express interest, please contact:

📩 Dr. Beata Nowakowska

[email protected]

Your support in reaching potential participants is invaluable. Together, we can make a lasting impact on the future of 22q11 research!

Thank you for your collaboration and dedication to the 22q11 community.