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
