Ask Me Anything: Precision Medicine for Rare Genetic Disorders
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Rare genetic disorders, often complex and challenging to diagnose, impact millions worldwide. Imagine a future where cutting-edge technology accelerates diagnosis, connects patients to life-changing treatments and empowers them with personalized care.
In this live "Ask Me Anything" session, Dr. Lukas Lange, CEO and co-founder of Probably Genetic, will answer your questions about the transformative power of precision medicine in addressing rare genetic disorders. With a unique blend of expertise spanning AI, bioinformatics and patient advocacy, Lukas offers invaluable insights into the latest advancements and the future of rare disease care.
Lukas will engage with our live audience on a range of topics related to precision medicine for rare genetic disorders. While the interactive nature of an AMA session means that every question can't be anticipated, we expect discussions will include:
- The vision behind Probably Genetic and its innovative approach to rare disease diagnosis.
- How AI, including Large Language Models (LLMs), is revolutionizing the identification and understanding of rare genetic conditions.
- The practical application of bioinformatics and at-home testing to accelerate patient diagnosis and connect them with relevant clinical trials.
- The challenges and opportunities in bringing rare disease drugs to market and the crucial role of patient advocacy in this process.
- The future of direct-to-consumer genetic testing and its implications for patient empowerment and personalized healthcare.
