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CGT (Carrier Genetic Test)



CGT is an advanced carrier genetic test before pregnancy, which determines whether a couple is a carrier of genetic mutations that could be transmitted to their children.

It analyses disorders such as Cystic Fibrosis, Spinal Muscular Atrophy, Fragile-X Syndrome amongst others by NGS.


  • Study on more than 6,000 mutations associated with over 600 genetic disorders.
  • Genetic counseling for patients and specialists.
  • Availability of a specific module for gamete donation programs.
  • Genetic screening test based on massive sequencing (NGS) and clinically validated.


  • For any couple who wants to form a family to know the risk of transmitting hereditary disorders to their children.
  • Before an assisted reproduction treatment.
  • Before a treatment with donor sperm or eggs.

Most carriers of genetic mutations don’t have a family history of these disorders.