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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

    Additionally, premutations must pass through females in order to transform into the full mutation. [2] Fragile X syndrome is so named because of the appearance of the X chromosome in individuals with fragile X. Under an electron microscope, a region on the long arm of the chromosome resembles a thin string.

  5. X-linked genetic disease - Wikipedia

    en.wikipedia.org/wiki/X-linked_genetic_disease

    Some X-linked dominant traits, such as Aicardi syndrome, cause embryonic death in males, leading them to appear only in born females who continue to survive with these conditions. Examples of X-linked dominant disorders include Rett syndrome , Fragile-X Syndrome , and the most cases in Alport syndrome .

  6. List of genetic disorders - Wikipedia

    en.wikipedia.org/wiki/List_of_genetic_disorders

    X-linked intellectual disability and macroorchidism (fragile X syndrome) X: X-linked spinal-bulbar muscle atrophy (spinal and bulbar muscular atrophy) X: Xp11.2 duplication syndrome Xp11.2: D [34] 1:1,000,000 X-linked severe combined immunodeficiency (X-SCID) X: X-linked sideroblastic anemia (XLSA) ALAS2 (X) 47,XXX (triple X syndrome) X C 1: ...

  7. 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.

  8. The best gifts to buy your grandkids — from babies to big ...

    www.aol.com/lifestyle/the-best-gifts-to-buy-your...

    UGG Women's Classic II Short Boot Chestnut . $160 at Walmart. Related articles. AOL. This 'Hallmark movie coat' is perfect for winter — and it's over $40 off. AOL.

  9. X-linked intellectual disability - Wikipedia

    en.wikipedia.org/wiki/X-linked_intellectual...

    Females with one affected X chromosome and one normal X chromosome tend to have milder symptoms. Unlike many other types of intellectual disability, the genetics of these conditions are relatively well understood. [2] [3] It has been estimated there are ~200 genes involved in this syndrome; of these ~100 have been identified. [4]