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Learn about Fragile X mental retardation syndrome through this 13-minute educational video that explores the genetic basis, clinical manifestations, and behavioral characteristics of this inherited disorder. Discover how mutations in the FMR1 gene lead to intellectual disability and developmental delays, while examining the specific intelligence and behavioral issues associated with Fragile X syndrome. Understand the molecular mechanisms underlying this X-linked genetic condition, including the role of CGG repeat expansions and their impact on protein production. Explore the characteristic physical features, cognitive patterns, and behavioral traits that define Fragile X syndrome, making it one of the most common inherited causes of autism spectrum disorders and intellectual disability. Gain insights into the diagnostic approaches, genetic counseling considerations, and current understanding of how FMR1 gene silencing affects neuronal development and synaptic function.
