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2 days ago · Fragile X syndrome is a genetic disorder which occurs as a result of a mutation of the Fragile X Messenger Ribonucleoprotein 1 (FMR1) gene on the X chromosome, most commonly an increase in the number of CGG trinucleotide repeats in the 5' untranslated region of FMR1.
Sep 26, 2024 · Assessment of individuals with fragile X syndrome (FXS) is challenging in numerous ways, ranging from choice and limitations of instruments, behavioral and emotional factors impacting the testing process, to scoring and interpretation.
Oct 9, 2024 · About one in 250 women and one in 600 men are carriers of the abnormal gene that causes Fragile X, with female carriers at a higher risk of early menopause. The syndrome is caused by an...
6 days ago · Fragile X syndrome causes a wide range of physical, mental and behavioural symptoms, including mild to severe intellectual disability. “ Common behavioural features include short attention...
6 days ago · Fragile X syndrome causes a wide range of physical, mental and behavioural symptoms, including mild to severe intellectual disability. “ Common behavioural features include short attention...
Oct 8, 2024 · In delivering a fragile X syndrome diagnosis, the strengths of those living with fragile X syndrome should be the starting point, encouraging development that builds on those strengths while supporting the areas of need.
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Sep 23, 2024 · Fragile-X syndrome, a chromosomal disorder associated with a fragile site on the end of the X chromosome. The major symptom of the syndrome is diminished mental ability, which may range from mild learning impairment to severe intellectual disability (or mental retardation).
