What developmental delays are commonly associated with Facile X Syndrome?

Facial X Syndrome, characterized by a mutation in the FMR1 gene, commonly leads to delays in speech and language development. Individuals with this condition often experience challenges with articulation, language processing, and overall communication skills due to cognitive impairments and social interaction difficulties. These language delays can vary in severity but typically manifest as a significant area of concern, making it a key feature of the syndrome.

While other developmental delays, such as those related to coordination, visual perception, and social skills, may also be present in individuals with Fragile X Syndrome, delays in speech and language are often viewed as among the most prominent and impactful. This focus on communication skills underscores the importance of targeted interventions and support in enhancing language development for these individuals.