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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. "Full trisomy", also called "primary trisomy", means that an entire extra chromosome has been copied. "Partial trisomy" means that there is an extra copy of part of a chromosome.

  3. Trisomy X - Wikipedia

    en.wikipedia.org/wiki/Trisomy_X

    Trisomy X, also known as triple X syndrome and characterized by the karyotype [note 1] 47,XXX, is a chromosome disorder in which a female has an extra copy of the X chromosome. It is relatively common and occurs in 1 in 1,000 females, but is rarely diagnosed; fewer than 10% of those with the condition know they have it.

  4. Down syndrome - Wikipedia

    en.wikipedia.org/wiki/Down_syndrome

    Down syndrome or Down's syndrome, 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. [1] [12] There are three types of Down syndrome, the ...

  5. Trisomy 18 - Wikipedia

    en.wikipedia.org/wiki/Trisomy_18

    Trisomy 18, also known as Edwards syndrome, is a genetic disorder caused by the presence of a third copy of all or part of chromosome 18. Many parts of the body are affected. [3] Babies are often born small and have heart defects . [3]

  6. Trisomy 8 - Wikipedia

    en.wikipedia.org/wiki/Trisomy_8

    Trisomy 8 mosaicism affects wide areas of chromosome 8, containing many genes, and can thus be associated with a range of symptoms. Mosaic trisomy 8 has been reported in rare cases of Rothmund–Thomson syndrome, a genetic disorder associated with the DNA helicase RECQL4 on chromosome 8q24.3. The syndrome is "characterized by skin atrophy ...

  7. Trisomy 16 - Wikipedia

    en.wikipedia.org/wiki/Trisomy_16

    Trisomy 16 is a chromosomal abnormality in which there are 3 copies of chromosome 16 rather than two. [1] It is the most common trisomy leading to miscarriage and the second most common chromosomal cause of it, closely following X-chromosome monosomy. [2] About 6% of miscarriages have trisomy 16. [3] Those mostly occur between 8 and 15 weeks ...

  8. Patau syndrome - Wikipedia

    en.wikipedia.org/wiki/Patau_syndrome

    Patau syndrome. Patau syndrome is a syndrome caused by a chromosomal abnormality, in which some or all of the cells of the body contain extra genetic material from chromosome 13. The extra genetic material disrupts normal development, causing multiple and complex organ defects. This can occur either because each cell contains a full extra copy ...

  9. Trisomy 22 - Wikipedia

    en.wikipedia.org/wiki/Trisomy_22

    Trisomy 22 is a chromosomal disorder in which three copies of chromosome 22 are present rather than two. It is a frequent cause of spontaneous abortion during the first trimester of pregnancy. Progression to the second trimester and live birth are rare. This disorder is found in individuals with an extra copy or a variation of chromosome 22 in ...