Trisomy 13 in the unborn child
Definition – what is a trisomy 13 in the unborn child? Trisomy 13, also called Pätau syndrome, is a change in the chromosomes in which chromosome 13 is present three times instead of twice. The disease is accompanied by malformations of several internal organs and can in many cases be detected before birth. Children born … Trisomy 13 in the unborn child