Did you know that fragile X syndrome is the most common inherited cause of intellectual disability in children ?
Fragile X Syndrome is the most common inherited cause of intellectual disability, often linked with learning challenges, speech delays, and features of autism.
It’s a genetic condition that often goes unnoticed in the early years.
Many children with Fragile X may have speech delays, difficulty with learning, social anxiety, or behaviors that overlap with autism and ADHD. Because these signs can vary from child to child, the diagnosis is sometimes delayed.
What makes Fragile X important to understand is that it doesn’t just affect learning, but it can influence how a child communicates, copes with change, and interacts with others.
Some children may struggle in classrooms or social settings, while others may experience emotional challenges that parents and teachers might not immediately connect to a genetic cause.
Early identification, therapies, and supportive environments can make a world of difference. With the right interventions, children with Fragile X can learn skills, build confidence, and thrive in their own unique ways.
Raising awareness is important because the earlier we recognize Fragile X, the better we can support both the child and their family.