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Fragile X Syndrome

Fragile X Syndrome

What is Fragile X Syndrome?

Fragile X Syndrome is an inherited disorder caused by changes within a gene (FMR1) that render it unable to produce a certain protein (FMRP) that is vital to normal brain development. Signs that a child might have Fragile X syndrome include Developmental delays (not sitting, walking, or talking at the same time as other children the same age); Learning disabilities (trouble learning new skills); and Social and behavior problems (such as not making eye contact, anxiety, trouble paying attention, hand flapping, acting and speaking without thinking, and being very active).