La enfermedad de Huntington: el dilema

The transcript discusses the decision-making process and implications of genetic testing for Huntington's disease. It highlights the cautious approach taken by genetic services due to potential mental health impacts. Personal reflections on testing are shared, including Brian's experience and results. The genetic inheritance of the disease is explained, emphasizing the 50% chance of passing the gene to offspring. The rarity of diseases caused by a single gene is also noted.

What are the implications of knowing whether one has the gene for Huntington's disease?

What are the emotional risks associated with receiving genetic test results?

Why might some individuals choose not to undergo genetic testing?

What was Brian's decision regarding genetic testing, and what was the outcome?

How does the inheritance of the Huntington's disease gene work among siblings?