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Transforming care for patients with rare diseases
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Dr. Tugce Balci
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Mar 10, 2026
Dr. Tugce Balci’s work at LHSC focuses on faster rare disease diagnosis, improved care, and access to research for children. The article highlights Kayden’s Kleefstra syndrome diagnosis, the role of tools like EpiSign™ in diagnosing 200+ genetic diseases, and the new SWORD program to support rare disease families and clinical trial access.
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