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INHERITED DISORDER SCREENING

PGT-M in Indore: Testing Embryos for Inherited Single-Gene Disorders

PGT-M tests IVF embryos for a known family genetic disease such as thalassaemia, so an unaffected embryo can be transferred. Learn the steps and accuracy.

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PGT-M (preimplantation genetic testing for monogenic disorders) helps couples who know they carry a serious inherited condition, such as beta-thalassaemia, sickle cell disease or spinal muscular atrophy, to have a baby who is not affected by that condition. At Asian Navkar Hospital, Indore, PGT-M is planned together with genetic counsellors and specialised genetic laboratories.

Who Is PGT-M For?

  • Couples where both partners are carriers of the same recessive disorder (for example, both thalassaemia carriers)
  • A partner with a dominant genetic condition
  • Families with an X-linked disorder
  • Couples who already have an affected child

A confirmed genetic diagnosis (the exact mutation) in the family is needed before testing can be designed.

Steps in PGT-M

  1. Genetic counselling and confirmation of the family mutation
  2. Creation of a test specific to your family (this can take several weeks)
  3. IVF with ICSI, embryo biopsy and freezing
  4. Transfer of an embryo reported as unaffected
  5. Confirmation by prenatal testing during pregnancy is recommended

Accuracy and Limits

PGT-M is highly accurate for the condition tested but is not perfect, and it does not test for other conditions. The number of unaffected embryos depends on the inheritance pattern and how many embryos are available.

Why Families Choose Asian Navkar Hospital, Indore

  • Fertility, embryology, high-risk obstetrics and a Level 3 NICU in one hospital, so care continues after a positive pregnancy test.
  • Senior IVF team with 30+ years of clinical experience, including clinical embryologists.
  • Counselling for both partners, transparent written estimates and cashless TPA/insurance desk support where policies allow.

Related Services

Medical References

This page is for general information and does not replace a consultation. Treatment decisions are made only after an in-person evaluation by a qualified doctor at Asian Navkar Hospital, Indore.

Condition-Specific Testing
Custom-designed test based on your family's genetic mutation.
Prevents Passing On Disorders
Helps avoid transmission of known inherited conditions.
Genetic Counselling Included
Guidance throughout the testing and decision process.
Works With Standard IVF
Performed as part of your existing IVF/ICSI cycle.

Is this for you?

✓ Known family history of a genetic disorder ✓ Both partners are carriers of the same condition ✓ Previous child affected by a genetic condition ✓ Identified single-gene mutation in the family

How We Treat PGT-M (Monogenic Disorder Testing)

1
Genetic Counselling
Understanding the specific condition and testing options.
2
Custom Test Design
A test is developed specifically for your family's mutation.
3
Embryo Biopsy
Cells are taken from embryos created through IVF/ICSI.
4
Selective Transfer
Unaffected embryos are identified and prioritized for transfer.

Frequently Asked Questions

If both parents are carriers, PGT-M can identify embryos not affected by thalassaemia major for transfer.

Yes. The exact mutations in the family must be known to design the test.

Test design can take several weeks; IVF and testing then follow. Your team will share a timeline.

Confirmation by CVS or amniocentesis is generally recommended.

No. Sex selection is illegal in India under the PC-PNDT Act.

Dr. Vedant Jain
Dr. Vedant Jain
MBBS, MS (Obs & Gynae), DNB • Consultant IVF Specialist, Gynecologist & Embryologist
Reg. No. MP-37997 (MP Medical Council)

Dr. Vedant Jain is an IVF Consultant, Gynecologist, and Certified Embryologist at Asian Navkar Hospital, Indore. Holding post-graduate degrees including an MS and DNB in Obstetrics and Gynecology, he practises reproductive medicine at Asian Navkar Hospital. Dr. Jain specializes in advanced Assisted Reproductive Technologies (ART), complex infertility assessments, low AMH (ovarian reserve) optimization, and fertility preservation. By combining clinical gynecology with laboratory embryology, he works with couples who have had unsuccessful IVF cycles to plan further evaluation and treatment.

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