Learn About Genetic Testing
Learn About Genetic Testing
Genetic testing provides the definitive diagnosis of TK2d.1
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Resources
Resources for TK2d and mitochondrial diseases
There are several resources for you and your patients when it comes to diagnosing and managing TK2d and other mitochondrial diseases.
Webinars
TK2d on-demand webinar (from live event May 2026)
Join our expert speakers, Prof Caterina Garone (chair), Dr Cristina Domínguez-González, Prof Thomas Klopstock, Prof Felix Distelmaier and Prof Edoardo Malfatti to learn more about TK2d, an ultra-rare mitochondrial disease.
This on-demand webinar features peer-to-peer discussions with internationally recognised experts on the evolving disease management landscape for people living with TK2d, a potentially life-threatening ultra-rare mitochondrial disease. Topics include the challenges of diagnosis, the role of genetic testing and the importance of timely referrals.
Patient Stories
Jared: Life beyond TK2d
Meet Jared, an aspiring science fiction writer with a master’s in quantum mechanics, and hear how he navigates his life beyond TK2d. Listen to his story.
Video Transcript
Jared Patient Testimonial Transcript
Connie: Misperceptions of TK2d
Meet Connie and learn how writing has empowered her to reclaim her narrative and address society’s misperceptions about TK2d. Listen to her story.
Video Transcript
Connie Patient Testimonial Transcript
TK2d Resources
TK2d Information From UMDF
Explore information about TK2d from the UMDF.
Clinical Trial Information
Learn how to participate in a clinical study or connect with a relevant research opportunity.
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GL-DA-2600754 | Date of preparation: July 2026