Children with rare conditions often face many challenges in getting the right diagnosis and treatment. They may have symptoms that are not well understood or recognized by the medical community, and they may have to undergo multiple tests and trials before finding a solution that works for them. Genomics can offer a ray of hope for these children and their families by providing accurate and timely information about their genetic makeup and how it affects their health.

In episode 16 of Genomics Gupshup, we have a candid conversation with Dr. Puja Grover Kapoor, a renowned pediatric neurologist. She gives us insights into pediatric care, the relationship between autism and epilepsy, and how genetic tests can be helpful for children with rare conditions. She also talks about the prevalence of autism in India, and when should a child undergo a genetic test.

If you want to learn more about how genomics can help children with rare conditions and improve their quality of life, don’t miss this episode of #genomicsgupshup!