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IIt takes a lot of patience, time and attention. Lots of therapy home and professional can help someone with fragile x to speak and do some small semi normal things.

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Fragile X syndrome is a genetic condition that causes a range of developmental problems including learning disabilities and cognitive impairment. Usually, males are more severely affected by this disorder than females. Affected individuals usually have delayed development of speech and language by age 2.

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poor muscle tone
gastric reflex
common ear infections
crawling, walking, and talking delayed development.

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learning disabilities
cognitive impairment
autistic behaviors
hyperactivity

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If a male carrier has a daughter with an unaffected female she will have the gene but only be a carrier. if the same people have a son the son will always be unaffected. If an unaffected male and carrier female have a child then the children, male of female will have a 50% chance of being affected either carrier or actually having it.

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The worlds most common inherited cause of mental imparement

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The worlds most common inherited cause of mental imparement

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The fmr1 gene responsible for producing a protein vital for normal brain development. This is normally made of up to 44 repeats of the cgg sequence in the gene. Some people with this gene may contain from 55-200 repeats making them a carrier. This is a fragile x pre mutation aka a carrier who is unaffected. in someone with over 200 repeats this stops the fmr1 gene from producing its necessary protein for proper brain growth.

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The Fragile X Association of Australia is a non-profit organisation that provides support to families living with Fragile X. This includes specialised clinics, mobile workshops, counselling and casework, fundraising and working to increase public awareness of Fragile X