chromosomes

The latest in pre-implantation genetic diagnosis (PGD)

Pre-implantation genetic diagnosis(PGD) consists of studying chromosomalabnormalities and genetic abnormalities in the embryo prior to transfer to the mother. Itspurpose is to ensure that children are healthy and to bring thetransmission of a given condition to an end.

Significant progress that has revolutionised this area ofreproductive medicine has been made over the last few years and specificallywith regards to one type […]

2018-12-17T18:43:53+02:0028 de December de 2018|0 Comments

Can we avoid the Genetic Ammiocentesis?

Genetic Amniocentesis is a prenatal diagnostic technique aimed at obtaining fetal karyotype. The karyotype is the number of chromosomes that are endowed with all people. Normal people we have 46 chromosomes distributed in 23 pairs (22 pairs of chromosomes called autosomes and 1 pair of sex chromosomes, XX or XY, which determine the sex of the fetus). Down syndrome or trisomy 21 is the most common chromosomal abnormality in new born infants; in this case, the individual has 47 chromosomes, and the alteration is that there are 3 21 chromosomes rather than two. […]

2014-07-16T13:41:57+02:004 de August de 2014|0 Comments
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