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  2. Distal trisomy 10q - Wikipedia

    en.wikipedia.org/wiki/Distal_trisomy_10q

    In Distal Trisomy 10q disorder, end or distal portion of the q (long) arm of the chromosome number 10 appears to be present three times, rather than two times as it is supposed to be. This extra arm results in chromosome 10 trisomy, meaning that three arms are present. Depending on the length of the aberrant arm, the severity can vary from case ...

  3. Pallister–Killian syndrome - Wikipedia

    en.wikipedia.org/wiki/Pallister–Killian_syndrome

    The Pallister–Killian syndrome (PKS), also termed tetrasomy 12p mosaicism or the Pallister mosaic aneuploidy syndrome, is an extremely rare and severe genetic disorder. PKS is due to the presence of an extra and abnormal chromosome termed a small supernumerary marker chromosome (sSMC). sSMCs contain copies of genetic material from parts of ...

  4. 17q12 microdeletion syndrome - Wikipedia

    en.wikipedia.org/wiki/17q12_microdeletion_syndrome

    17q12 microdeletion syndrome, also known as 17q12 deletion syndrome, is a rare chromosomal anomaly caused by the deletion of a small amount of material from a region in the long arm of chromosome 17. It is typified by deletion of the HNF1B gene, resulting in kidney abnormalities and renal cysts and diabetes syndrome. It also has neurocognitive effects, and has been implicated as a genetic ...

  5. Mouse models of Down syndrome - Wikipedia

    en.wikipedia.org/wiki/Mouse_models_of_Down_syndrome

    Background Trisomy 21, an extra copy of the 21st chromosome, is responsible for causing Down syndrome, and the mouse chromosome 16 closely resembles human chromosome 21. [1] In 1979, trisomy of the mouse chromosome 16 (Ts16) initially showed potential to be a model organism for human Down syndrome. [2] However, Ts16 embryos rarely survive until birth, making them unable to serve as a model for ...

  6. Trisomy X - Wikipedia

    en.wikipedia.org/wiki/Trisomy_X

    Trisomy X occurs via a process called nondisjunction, in which normal cell division is interrupted and produces gametes with too many or too few chromosomes. Nondisjunction is a random occurrence, and most girls and women with trisomy X have no family histories of chromosome aneuploidy. [note 2] Advanced maternal age is mildly associated with trisomy X. Women with trisomy X can have children ...

  7. Woman, 102, who still works 3 days a week shares simple ... - AOL

    www.aol.com/news/woman-102-still-works-3...

    Woman, 102, who still works 3 days a week shares simple advice for living a long life Ella Jeffries July 8, 2024 at 3:03 PM

  8. Patau syndrome - Wikipedia

    en.wikipedia.org/wiki/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.

  9. Jasmine Paolini reaches her second consecutive Grand Slam ...

    www.aol.com/news/jasmine-paolini-reaches-her...

    Jasmine Paolini reached her second consecutive Grand Slam final with a 2-6, 6-4, 7-6 (10-8) victory over unseeded Donna Vekic at Wimbledon on Thursday in a rollicking match that lasted 2 hours, 51 ...

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