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  2. Fragile X syndrome - Wikipedia

    en.wikipedia.org/wiki/Fragile_X_syndrome

    Fragile X syndrome (FXS) is a genetic neurodevelopmental disorder characterized by mild-to-moderate intellectual disability. [1] The average IQ in males with FXS is under 55, while about two thirds of affected females are intellectually disabled.

  3. Fragile X-associated primary ovarian insufficiency - Wikipedia

    en.wikipedia.org/wiki/Fragile_X-associated...

    Fragile X-associated primary ovarian insufficiency (FXPOI) is the most common genetic cause of premature ovarian failure in women with a normal karyotype 46,XX. [1] The expansion of a CGG repeat in the 5' untranslated region of the FMR1 gene from the normal range of 5-45 repeats to the premutation range of 55-199 CGGs leads to risk of FXPOI for ovary-bearing individuals. [2]

  4. Sherman paradox - Wikipedia

    en.wikipedia.org/wiki/Sherman_paradox

    Sherman theorized that the gene responsible for fragile X syndrome becomes mutated through a two-step process. The first mutation, called the 'premutation', doesn't cause any clinical symptoms. A second mutation was required to convert the 'premutation' into a 'full mutation' capable of causing the clinical symptoms associated with fragile X ...

  5. Fragile X-associated tremor/ataxia syndrome - Wikipedia

    en.wikipedia.org/wiki/Fragile_X-associated...

    Fragile X-associated tremor/ataxia syndrome (FXTAS) is a late-onset neurodegenerative disorder most frequently seen in male premutation carriers of Fragile X syndrome (FXS) over the age of 50. [ 4 ] [ 5 ] The main clinical features of FXTAS include problems of movement with cerebellar gait ataxia and action tremor .

  6. FMR1 - Wikipedia

    en.wikipedia.org/wiki/FMR1

    FMR1 (Fragile X Messenger Ribonucleoprotein 1) is a human gene [5] that codes for a protein called fragile X messenger ribonucleoprotein, or FMRP. [6] This protein, most commonly found in the brain, is essential for normal cognitive development and female reproductive function.

  7. Chromosomal fragile site - Wikipedia

    en.wikipedia.org/wiki/Chromosomal_fragile_site

    Silencing of the FMR1 gene in Fragile X syndrome. FMR1 co-localizes with a rare fragile site, visible here as a gap on the long arms of the X chromosome.. A chromosomal fragile site is a specific heritable point on a chromosome that tends to form a gap or constriction and may tend to break [1] when the cell is exposed to partial replication stress. [2]

  8. Category:Neurogenetic disorders - Wikipedia

    en.wikipedia.org/wiki/Category:Neurogenetic...

    Download QR code; Print/export Download as PDF; Printable version; In other projects Wikimedia Commons; Wikidata item; Appearance. ... Fragile X syndrome; H.

  9. FXS - Wikipedia

    en.wikipedia.org/wiki/FXS

    Download as PDF; Printable version; In other projects Wikidata item; Appearance. move to sidebar hide ... Fragile X syndrome, genetic disorder; Toyota FXS, concept ...