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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 virtually any other chromosome and, depending on the ...

  4. Chromosome abnormality - Wikipedia

    en.wikipedia.org/wiki/Chromosome_abnormality

    Chromosome abnormality A chromosomal abnormality, chromosomal anomaly, chromosomal aberration, chromosomal mutation, or chromosomal disorder is a missing, extra, or irregular portion of chromosomal DNA. [1] [2] These can occur in the form of numerical abnormalities, where there is an atypical number of chromosomes, or as structural abnormalities, where one or more individual chromosomes are ...

  5. Marker chromosome - Wikipedia

    en.wikipedia.org/wiki/Marker_chromosome

    Marker chromosomes typically occur in addition to the standard 46 chromosomes, making it a partial trisomy or tetrasomy supernumerary chromosome. [4] A marker can be composed of inactive genetic material and have little or no effect, or it can carry active genes and cause genetic conditions such as iso (12p), which is associated with Pallister-Killian syndrome, and iso (18p), which is ...

  6. Chromosome 10 - Wikipedia

    en.wikipedia.org/wiki/Chromosome_10

    Chromosome 10 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. Chromosome 10 spans about 134 million base pairs (the building material of DNA) and represents between 4 and 4.5 percent of the total DNA in cells .

  7. Cat eye syndrome - Wikipedia

    en.wikipedia.org/wiki/Cat_eye_syndrome

    Cat-eye syndrome (CES) or Schmid–Fraccaro syndrome is a rare condition caused by an abnormal extra chromosome, i.e. a small supernumerary marker chromosome. [2] This chromosome consists of the entire short arm and a small section of the long arm of chromosome 22. In consequence, individuals with the cat-eye syndrome have three ( trisomic) or four ( tetrasomic) copies of the genetic material ...

  8. Aneuploidy - Wikipedia

    en.wikipedia.org/wiki/Aneuploidy

    The terms "partial monosomy" and "partial trisomy" are used to describe an imbalance of genetic material caused by loss or gain of part of a chromosome. In particular, these terms would be used in the situation of an unbalanced translocation, where an individual carries a derivative chromosome formed through the breakage and fusion of two ...

  9. About 4% of US adults age 65 and older have a dementia ...

    www.aol.com/news/4-us-adults-age-65-040225251.html

    (Reuters) - Some 4% of U.S. adults aged 65 and older say they have been diagnosed with dementia, a rate that reached 13% for those at least 85-years old, according to a report of a national survey ...

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