Understanding Fragile X Syndrome: Genetics, Clinical Insights, and Interventions - Webinar - May 22, 1:00-2:30 p.m. (MT)

Thursday, May 22, 2025
1:00-2:30 PM (MT)

This webinar provides a comprehensive introduction to Fragile X syndrome, the most common inherited cause of intellectual disability and a leading known genetic cause of autism. Designed for healthcare professionals, therapists, and families, this session will cover the basic genetics and inheritance patterns of Fragile X, key clinical features across the lifespan, its connection to autism, and current approaches to treatment and support. Attendees will gain foundational knowledge to better identify, understand, and support individuals with Fragile X syndrome. 

Learning Objectives:

• Explain the genetic basis of Fragile X syndrome, including FMR1 gene mutations and inheritance patterns.
• Identify common clinical features of Fragile X across developmental stages, including cognitive, behavioral, and physical characteristics.
• Describe the relationship between Fragile X syndrome and autism.
• Discuss current treatment options, including behavioral, educational, and pharmacologic interventions.
• Recognize the importance of family education and genetic counseling in the management and support of individuals with Fragile X.

Speakers: 

• Nicole Tartaglia, MD, MS; Professor, Developmental Pediatrics, University of Colorado School of Medicine; Medical Director, Denver Fragile X Clinic
• Susan Howell, MS, CGC; Associate Professor, Genetics & Metabolism, University of Colorado School of Medicine; Genetic Counselor, Denver Fragile X Clinic

Intended Audience: Healthcare professionals, therapists, educators, psychologists, and families

Accommodations, including captioning and Spanish interpretation, may be requested during registration. Accommodation requests should be submitted no later than May 12, 2025.

Questions may be directed to Christine Cook at christine.cook@cuanschutz.edu.