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Rare Genomes Project: Hannah Tansey’s story

Hannah Tansey is a young woman living with Kleefstra Syndrome Type 2. She and her parents started working with the Rare Genomes Project in 2017. Hannah received her diagnosis in 2018 at the age of 23. In this video, her mother, Tammy, talks about the journey of Hannah and her family.

For more information visit: https://www.RareGenomes.org