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Trisomy 16

Trisomy 16

Partial or complete triplication of chromosome 16.

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Readers' pathsAug 2026 – Oct 2026

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  1. Mosaic (genetics)

    Possession of multiple genetic lineages within a multi-cellular organism.

    18%

  2. Turner syndrome

    X chromosome monosomy.

    13%

  3. Chromosome 16

    Human chromosome.

    10%

  4. Atrial septal defect

    Human heart defect present at birth.

    9%

  5. Spina bifida

    Birth defect of the spinal cord.

    8.8%

  6. Camptodactyly

    Permanent bending of a finger or toe.

    8.5%

  7. Hypospadias

    Malformation in which the urethral opening is misplaced.

    7.6%

  8. Chromosome abnormality

    Abnormal number or structure of chromosomes.

    3.8%

  9. Chorionic villus sampling

    Prenatal genetic disorder test.

    1.7%

  10. Miscarriage

    Natural premature termination of pregnancy.

    1.6%

Readers come from

Share of the 1,949 readers arriving from another article

  1. Trisomy

    Abnormal presence of three copies of a particular chromosome.

    23%

  2. Aneuploidy

    Presence of an abnormal number of chromosomes in a cell.

    9.5%

  3. Chromosome 16

    Human chromosome.

    6.2%

  4. Patau syndrome

    Chromosomal disorder in which there are three copies of chromosome 13.

    0.92%

  5. Trisomy 18

    Chromosomal disorder in which there are three copies of chromosome 18.

    0.62%