What is a Genetic Carrier? Understanding Your Carrier Status | jscreen скачать в хорошем качестве

What is a Genetic Carrier? Understanding Your Carrier Status | jscreen

Join Karen Grinzaid with jscreen as she explains what it means to be a genetic carrier. Learn about: • How carriers have one normal and one mutated gene copy • Why most carriers are healthy and show no symptoms • The 25% risk when both parents are carriers • Common conditions like cystic fibrosis, sickle cell anemia, Tay-Sachs • Why carrier status matters for family planning Being a carrier is actually quite common - most people are carriers for one or more genetic conditions! To learn more about what a Genetic Carrier is, read our blog on it: https://www.jscreen.org/blog/what-is-... Visit jscreen.org to learn more about carrier screening and testing options. #GeneticCarrier #CarrierStatus #GeneticTesting #FamilyPlanning #GeneticCounseling #jscreen today we're exploring what it means to be a carrier of a genetic disease. A carrier is an individual who has one copy of a gene mutation associated with a recessive genetic disorder, but typically doesn't show symptoms of the condition. Here's what you need to know: 1. Carriers have one normal copy and one mutated copy of a gene for a recessive condition. 2. Most carriers are healthy and never know they carry the mutation. 3. When both parents are carriers of the same recessive condition, there's a 25% chance with each pregnancy that their child will inherit both mutations and develop the condition. 4. Being a carrier is actually quite common. Most people are carriers for one or more genetic conditions. 5. Carrier screening can identify if you're a carrier for certain genetic conditions. 6. Carrier status is most relevant when planning a family, as it can inform reproductive decisions. 7. People can be carriers for various conditions, including cystic fibrosis, sickle cell anemia, and Tay-Sachs disease, among others. It's important to understand that being a carrier doesn't mean you have the genetic condition or that you'll develop it. It simply means you have the potential to pass the mutation to your children. If you're found to be a carrier, it's important that your partner also undergo testing, especially if you're planning a pregnancy. This can help assess the risk of having a child with the genetic condition. Remember, being a carrier is not a diagnosis and is generally not a health problem. It's information that can be valuable for family planning and, in some cases, for your own health management. If you have questions about your carrier status or are considering carrier screening, visit jscreen.org.