An amniocentesis or amniotic fluid test has identified a defect on the short arm of the 21st pair of chromosomes in a developing embryo. it is likely that this child will have

In this question, the child would likely to have a down syndrome. Down Syndrome is a genetic disorder that shows the presence of the three number 21 chromosomes. Down syndrome is also known as Trisomy 21. This disorder is the most common abnormalities / disorders in people and down syndrome has no cure.