Pediatric Genetic Disorders and Rare Diseases

This session will focus on the diagnosis and management of rare genetic disorders in children, including metabolic diseases, chromosomal abnormalities, and syndromes with developmental delays. Advances in genetic screening, gene therapy, and personalized medicine will be discussed. The role of genetic counseling and family support will also be highlighted, ensuring that attendees leave with a comprehensive understanding of how to care for children with rare and complex genetic conditions.

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