Prenatal & Reproductive Genetics
An ultrasound shows what. Genetics explains why.
Clinical genetics is not an add-on to this practice — it is its centre. Understanding the underlying cause guides diagnosis, management, counselling and every future pregnancy decision.
Why Clinical Genetics Matters
Understanding the cause changes what happens next.
Two families can receive the same scan finding and need entirely different care. What separates them is the cause.
Understanding the cause helps with
- Accurate diagnosis
- Choosing the appropriate genetic tests
- Pregnancy management decisions
- Recurrence risk assessment
- Future pregnancy planning
- IVF and reproductive planning
- Family counselling and testing of relatives
Pregnancy complications may be associated with
Identifying which of these applies is essential for appropriate treatment and future planning.
- Chromosomal abnormalities
- Single-gene disorders
- Carrier status in healthy parents
- Maternal age
- Family history
- Previous pregnancy loss
- Recurrent IVF failure
- Inherited disorders
- New (de novo) genetic changes
Services
Genetics across the whole reproductive journey.
From before conception through prenatal diagnosis to planning the next pregnancy.
Genetic Counselling
A structured conversation about risk, testing options and what each result would mean.
Carrier Screening
Identifying healthy carriers of recessive conditions before or during pregnancy.
Preconception Counselling
Evaluation and planning before conception, when every option is still open.
Prenatal Genetics
Test selection and interpretation for pregnancies with abnormal scans or screening.
Embryo Genetics
Understanding embryo chromosome status and its implications for transfer.
PGT Counselling
PGT-M, PGT-SR and PGT-A explained, and whether they apply to your situation.
Recurrent Pregnancy Loss
Genetics-led evaluation after two or more losses.
Recurrent IVF Failure
Assessment of embryonic, parental and uterine contributors.
Advanced Maternal Age
Age-specific risk assessment and appropriate testing pathways.
Family History Assessment
Pedigree analysis to identify inherited patterns and at-risk relatives.
Prenatal Diagnostic Testing
CVS and amniocentesis performed with image-guided precision.
Interpretation of Genetic Reports
Karyotype, microarray, exome and panel reports translated into plain language.
Next Step
Bring your reports. We'll find the cause together.
Consultations at Apollo Cradle, Apollo Fertility, AIFMRG and Epic International, Hyderabad.