PGD Team Work
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Ms. Asmaa Alaidaroos
Lab Specialist
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Ms. Sawsan Abuzinadah
Lab Technician
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Ms. Rukhaa Chaudhary
Lab Specialist
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Ms. Bayan Aslani
Lab Specialist
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Mr. Mohammed Aloufi
Lab Specialist
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Pre-implantation Genetic Diagnosis (PGD)
Pre-implantation genetic diagnosis (PGD) is a procedure
used prior to implantation to help identify genetic defects
within embryos created through In Vitro Fertilization to
prevent certain diseases or disorders from being passed on
to the child.
In Vitro Fertilization (IVF)
In Vitro Fertilization includes egg retrieval and fertilization
in the lab. The developing embryos on the third day (10-8
cell stage) are genetically screened. Then healthy embryos
are transferred to the mother.
Comprehensive Test of Chromosomes
(PGD/PGS )
Preimplantation genetic screening PGS can benefit any
couple at risk for passing on chromosomal abnormalities.
Who are the recommended cases for
PGD/PGS/IVF?
- Sickle cell anemia, Thalassemia and single- gene
disorders with confirmed pathogenic mutation.
- If the affected gene is known, a custom PGD protocol will
be designed and implemented.
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If the affected gene is unknown to the couple, whole-exome
sequencing will be orered to them to maximize the
chances of identifying the underlying mutation.
- Recurrent Abortions/Miscarriages (Normal karyotype).
- Recurrent IVF failure (3/2 or more).
- Advance Maternal Age (>38/35).
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(PGD-IVF) Steps
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Last Update
10/4/2021 9:06:00 AM
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