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Fragile X is a genetic abnormality which is inherited and individuals therefore have the condition from birth, although, depending on the severity of the symptoms it is often undetected until early childhood. The average age of diagnosis is 8 years old. If however, parents are known to be carriers of Fragile X, the child may be given a blood test early on which is used to diagnose fragile x.

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15y ago
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11y ago

When? At conception. How? when a change or mutation to single a gene.

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14y ago

Fragile X Syndrome is a birth defect.

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14y ago

no, FXS begins while a fetus.

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14y ago

it is apparent at birth.

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Q: Is there a certain age for fragile x syndrome to occur?
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