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  2. 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. In humans, there are 23 chromosomes, but ...

  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. 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 ...

  5. Aneuploidy - Wikipedia

    en.wikipedia.org/wiki/Aneuploidy

    Specialty. Medical genetics. Aneuploidy is the presence of an abnormal number of chromosomes in a cell, for example a human cell having 45 or 47 chromosomes instead of the usual 46. [1] [2] It does not include a difference of one or more complete sets of chromosomes. A cell with any number of complete chromosome sets is called a euploid cell.

  6. Ring chromosome 20 syndrome - Wikipedia

    en.wikipedia.org/wiki/Ring_chromosome_20_syndrome

    Ring chromosome 20 syndrome. Ring chromosome 20, ring-shaped chromosome 20 or r (20) syndrome is a rare human chromosome abnormality where the two arms of chromosome 20 fuse to form a ring chromosome. The syndrome is associated with epileptic seizures, behaviour disorders and intellectual disability. [1]

  7. Living with trisomy 18: How a 6-year-old girl is beating the odds

    www.aol.com/living-trisomy-18-6-old-201618650.html

    Trisomy 18 typically results in life-threatening complications for a baby, but one little girl, Georgia, is proof of how one can live with it. Living with trisomy 18: How a 6-year-old girl is ...

  8. Cri du chat syndrome - Wikipedia

    en.wikipedia.org/wiki/Cri_du_chat_syndrome

    Cri du chat syndrome. Cri du chat syndrome is a rare genetic disorder due to a partial chromosome deletion on chromosome 5. [1] Its name is a French term ("cat-cry" or "call of the cat") referring to the characteristic cat-like cry of affected children (sound sample [1] ). [2] It was first described by Jérôme Lejeune in 1963. [3]

  9. Gestational trophoblastic disease - Wikipedia

    en.wikipedia.org/wiki/Gestational_trophoblastic...

    Oncology. Gestational trophoblastic disease ( GTD) is a term used for a group of pregnancy-related tumours. [1] These tumours are rare, and they appear when cells in the womb start to proliferate uncontrollably. The cells that form gestational trophoblastic tumours are called trophoblasts and come from tissue that grows to form the placenta ...

  1. Related searches partial trisomy 10q results range table for babies and children 20 years

    distal trisomy 10qtrisomy 16 autosomal
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    full trisomy 13trisomy 21 and patau syndrome
    trisomy 13 wiki