Health Talks — Rare Genetic Disorders: Targeted Support from Diagnosis to Therapy

Rare genetic disorders, once difficult to diagnose, have seen significant advancements through genomics, enabling precise diagnoses and the development of targeted therapies, as demonstrated by the successes in treating conditions like spinal muscular atrophy and Duchenne muscular dystrophy. Our health experts will provide an overview of the prevalence of rare genetic disorders and the current diagnostic approaches, while also examining the broader implications for treatment and patient care. We will highlight the ongoing research at TGen’s Center for Rare Childhood Disorders with a particular focus on gene therapy studies related to Rett syndrome. Join us for a one-hour webinar and get up to date on approaches and options available for rare genetic disorders.

Dr. Vinodh Narayanan

Medical director, Center for Rare Childhood Disorders 

Translational Genomics Research Institute

Keri Ramsey

Clinical co-director, Center for Rare Childhood Disorders

Translational Genomics Research Institute

Katherine Hunt Brendish, moderator

Clinical professor and genetic counseling program director

ASU College of Health Solutions