Genetic screening, on the other hand, involves testing a person's DNA to identify genetic mutations or variations that might predispose them to certain diseases or conditions. In the context of cancer, for instance, screening can detect mutations in genes like BRCA1 and BRCA2 that significantly increase the risk of breast, ovarian, and other cancers. By identifying these genetic markers early, healthcare providers can recommend tailored monitoring, preventive surgeries, or medications that may lower the risk of developing cancer. Additionally, genetic screening can play a critical role in guiding personalized treatments, helping doctors select the most effective therapies based on an individual's genetic makeup. Together, genetic counseling and screening empower patients with the knowledge to make proactive health decisions and manage potential risks before they become life-threatening.
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