Genetic counselling to determine if the couple needs genetic test of the embryo & which type of test should be done .
Personal or family history of single-gene defects—such as cystic fibrosis, haemophilia, sickle cell anaemia, muscular dystrophy, citrullinemia , multiple exostosis etc.
In known carriers of chromosomal structural rearrangement normal embryos can be selected by PGT SR.
The aim of this discussion is to make anyone with curious mind to understand these condition better. It is not equivalent to detailed in person individualised consultation.
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