Fragile X Syndrome

Fragile X chromosome syndrome is a genetic condition that affects development and is a known hereditary cause of learning difficulties. It originates from an alteration in a gene on the X chromosome and can manifest in different ways.

Common characteristics: delays in language and learning development, attention difficulties, anxiety, and, at times, particular physical features.

When to consult? When delays in development or language that warrant evaluation are observed.

Which specialist treats it? The pediatrician coordinates the developmental assessment, the speech therapist supports language, and the psychologist and the educational psychologist support learning and behavior. A team approach makes it possible to offer appropriate support to each child and their family.