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PGD

PGD

Preimplantation genetic diagnosis-further divides in to two categories
PGT-M and PGT-SR


PGT -M

PGTM, or preimplantation genetic testing for mutatationwas formerly known as preimplantation genetic diagnosis (PGD).PGT-M detects single gene defects or monogeneicdisorders. PGT-M,is mainly for people who know that they are at an increased risk of passing a specific genetic condition to their children.


Indications:


It is for people who are carriers for an autosomal recessive condition (Eg: Thalassemia)

Women who are carriers for X linked condition( Eg: Duchenne muscular dystrophy)

Either you or your partner are affected with an autosomal dominant condition. (Eg: Marfan syndrome)

You had a child or pregnancy with a single gene disorder


PGT-SR

PGT-SR, or preimplantation genetic testing for chromosomal structural rearrangements. It is a genetic testing for structural chromosomal rearrangements, which can be performed to improve the possibility of establishing a healthy pregnancy.
People with chromosome rearrangements are at an50% risk of producing embryos with an incorrect amount of genetic material, resulting in deletion/ duplication syndrome which typically does not lead to a successful pregnancy.

It is recommendedfor people with

Carriers of balanced translocation, Robertsonian translocation


Pre PGT work up :


ICSI followed by embryo culture

Embryo biopsy

Screened for PGT-A/PGT-M/PGT-SR

Embryo transfer: Transfer of a genetically healthy embryo

DAY 1 FERTILISED EMBRYO




DAY 2 CLEAVAGEMBRYO




DAY 3 CLEAVAGE EMBRYO






DAY 5 BLASTO CYST






Embryo biopsy






Embryo biopsy










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