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  2. Trisomy - Wikipedia

    en.wikipedia.org/wiki/Trisomy

    The number of chromosomes in the cell where trisomy occurs is represented as, for example, 2n+1 if one chromosome shows trisomy, 2n+1+1 if two show trisomy, etc. [2] "Full trisomy", also called "primary trisomy", [2] means that an entire extra chromosome has been copied. "Partial trisomy" means that there is an extra copy of part of a chromosome.

  3. Genetics of Down syndrome - Wikipedia

    en.wikipedia.org/wiki/Genetics_of_Down_syndrome

    An anaphase lag of a chromosome 21 in a Down syndrome embryo leads to a fraction of euploid cells (2n cells), phenomenon described as "aneuploidy rescue". There is considerable variability in the fraction of cells with trisomy 21, both as a whole and tissue-by-tissue. This is the cause of 1–2% of the observed Down syndromes. [4]

  4. Distal trisomy 10q - Wikipedia

    en.wikipedia.org/wiki/Distal_trisomy_10q

    Distal trisomy 10 is a rare chromosomal disorder that causes several physical defects and intellectual disability. [5] Humans, like all sexually reproducing species, have somatic cells that are in diploid [2N] state, meaning that N represent the number of chromosomes, and 2 the number of their copies.

  5. What is trisomy 18? Why the fatal genetic disorder is in the ...

    www.aol.com/lifestyle/trisomy-18-why-fatal...

    Trisomy 18 — also known as Edwards syndrome — is a chromosomal condition that is fatal in all but very rare cases, ... This test takes a small sample of cells from the placenta to look for ...

  6. Aneuploidy - Wikipedia

    en.wikipedia.org/wiki/Aneuploidy

    Trisomy 18 (Edwards syndrome) affects 1 in 6,000 births, and trisomy 13 (Patau syndrome) affects 1 in 10,000 births. 10% of infants with trisomy 18 or 13 reach 1 year of age. [ 9 ] Changes in chromosome number may not necessarily be present in all cells in an individual.

  7. Down syndrome - Wikipedia

    en.wikipedia.org/wiki/Down_syndrome

    Down syndrome or Down's syndrome, [12] also known as trisomy 21, is a genetic disorder caused by the presence of all or part of a third copy of chromosome 21. [3] It is usually associated with developmental delays, mild to moderate intellectual disability , and characteristic physical features.

  8. Mosaic (genetics) - Wikipedia

    en.wikipedia.org/wiki/Mosaic_(genetics)

    Gonosomal mosaicism is a type of somatic mosaicism that occurs very early in the organisms development and thus is present within both germline and somatic cells. [1] [22] Somatic mosaicism is not generally inheritable as it does not usually affect germ cells. In the instance of gonosomal mosaicism, organisms have the potential to pass the ...

  9. Trisomy 8 - Wikipedia

    en.wikipedia.org/wiki/Trisomy_8

    Complete trisomy 8 causes severe abnormalities in the developing fetus and can be a cause of miscarriage. [2] [3] Complete trisomy 8 is usually a gestational lethal condition, whereas trisomy 8 mosaicism is less severe and individuals with a low proportion of affected cells may exhibit a comparatively mild range of physical abnormalities and developmental delay. [4]