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  2. Ring chromosome 18 - Wikipedia

    en.wikipedia.org/wiki/Ring_chromosome_18

    The ring is formed when the caps on both the long arm (q) and the short arm (p) of one copy of chromosome 18 are lost and the new ends re-join to form the ring. Because the ring involves deletions of both the long arm (18q-) and the short arm (18p-) of chromosome 18, individuals with ring 18 can have features of both 18p-as well as distal 18q-.

  3. Distal 18q- - Wikipedia

    en.wikipedia.org/wiki/Distal_18q-

    Specialty. Medical genetics. Distal 18q- is a genetic condition caused by a deletion of genetic material within one of the two copies of chromosome 18. [1] The deletion involves the distal section of 18q and typically extends to the tip of the long arm of chromosome 18. [2]

  4. Proximal 18q- - Wikipedia

    en.wikipedia.org/wiki/Proximal_18q-

    Proximal 18q-is a rare genetic condition caused by a deletion of genetic material within one of the two copies of chromosome 18. This deletion involves the proximal (near the centromere ) section of the long arm of chromosome 18 somewhere between 18q11.2 (18.9 Mb) to 18q21.1 (43.8 Mb). [ 1 ]

  5. Trisomy 18 - Wikipedia

    en.wikipedia.org/wiki/Trisomy_18

    1 per 5,000 births [3] 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. [3] Many parts of the body are affected. [3] Babies are often born small and have heart defects. [3] Other features include a small head, small jaw, clenched fists with overlapping ...

  6. Chromosome 18 - Wikipedia

    en.wikipedia.org/wiki/Chromosome_18

    NC_000018 (FASTA) GenBank. CM000680 (FASTA) Chromosome 18 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. Chromosome 18 spans about 80 million base pairs (the building material of DNA) and represents about 2.5 percent of the total DNA in cells.

  7. Beckwith–Wiedemann syndrome - Wikipedia

    en.wikipedia.org/wiki/Beckwith–Wiedemann_syndrome

    1 in 10,000 [2] Beckwith–Wiedemann syndrome (/ ˈbɛkˌwɪθ ˈviːdə.mən /; abbreviated BWS) is an overgrowth disorder usually present at birth, characterized by an increased risk of childhood cancer and certain congenital features. A minority (<15%) of cases of BWS are familial, meaning that a close relative may also have BWS, and parents ...

  8. University of Pikeville Kentucky College of Osteopathic Medicine

    en.wikipedia.org/wiki/University_of_Pikeville...

    Website. upike.edu/COM. The University of Pikeville - Kentucky College of Osteopathic Medicine (UP-KYCOM) is the medical school of University of Pikeville, a private university affiliated with the Presbyterian Church (USA) and located in Pikeville, Kentucky. UP-KYCOM was established in 1997, grants the Doctor of Osteopathic Medicine degree.

  9. Monosomy - Wikipedia

    en.wikipedia.org/wiki/Monosomy

    Turner syndrome is the only full monosomy that is seen in humans — all other cases of full monosomy are lethal and the individual will not survive development. Cri du chat syndrome – (French for "cry of the cat" after the persons' malformed larynx ) a partial monosomy caused by a deletion of the end of the short arm of chromosome 5