embryo CCS

Can I choose the sex of my embryos when I undergo embryo transfer?

The human genome consists of 46 chromosomes: 23 of these are inherited from our father and the other 23 are inherited from our mother. Our organism’s entire genetic make-up is stored in these chromosomes. The 23 pairs are organised as follows: 22 pairs, known as autosomes, and one pair of sex chromosomes (X and Y) which differentiate the two sexes (XY for males and XX for females).
From a technical point of view, using pre-implantation genetic diagnosis, we have the means of analysing an embryo’s entire chromosomal make-up. This technique, which is known as PGS/PGT-A/CCS (Comprehensive Chromosome Screening), means additional or a lack of any chromosomes in the embryo can be detected. Therefore, we can use PGS/PGT-A/CCS to analyse the entire make-up of the embryo and determine that there are neither DNA excesses nor deficiencies which will stop the embryo from developing properly. But, if we focus on the sex chromosomes, we can also determine if the analysed embryo has two X chromosomes and will, therefore, be a girl (XX) or one X chromosome and one Y chromosome (XY) and will be a boy. […]

2018-03-26T19:17:10+02:0029 de July de 2016|0 Comments

Fertility research: one of a kind treatment for one of a kind patients

Research in the field of assisted reproduction provides us with more and more answers to situations which previously had none. It gives us solutions, options and new ways of overcoming the many difficulties which arise in reproduction.  What’s more, progress in science also helps diagnosis and treatment to be increasingly specific, personalised and individual. In fact, we might even say that the aim is to reach a point where one of a kind treatments are designed for one of a kind patients. […]

2018-03-26T18:11:08+02:0017 de July de 2015|0 Comments
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