Triploid Syndrome

From Wikipedia, the free encyclopedia

A Karyotype of a person who has this genetic disorder.
A Karyotype of a person who has this genetic disorder.

Triploid Syndrome is an extremely rare chromosomal disorder. Individuals with triploid syndrome have three of every chromosome for a total of sixty-nine rather than the normal forty-six chromosomes. Babies with Triploid Syndrome usually are lost through early miscarriage. However, some infants have been born and survived as long as five months. Affected infants are usually small and have multiple birth defects. Those that survive are usually mosaic, meaning that some cells have the normal number of 46 chromosomes and some cells have a complete extra set of chromosomes.


  • Chromosome Triploidy Syndrome
  • Triploidy
  • Triploidy Syndrome
  • 3n Syndrome
  • Diploid/Triploid Mixoploidy
  • 2n/3n Mixoploidy


The main article for this category is Syndrome.
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