Our Comprehensive Services
1. Reproductive Genetics & Pregnancy Loss Evaluation
Recurrent miscarriage or infertility can often have a genetic basis. Our specialists perform comprehensive evaluations including:
- Chromosomal analysis of both partners
- Genetic screening for recurrent pregnancy loss
- Evaluation for balanced translocations
- Guidance on future pregnancy planning
These services help couples understand causes, reduce recurrence risk, and improve pregnancy outcomes.
2. Prenatal Screening & Fetal Medicine Diagnostics
We provide a full range of prenatal genetic evaluations to detect abnormalities at the earliest stages of pregnancy.
• Maternal Serum Screening
- Dual marker test
- Triple marker test
- Quadruple marker test
These screens assess risk for chromosomal disorders such as Down syndrome and neural tube defects.
• Ultrasound Soft Marker Assessment
- Echogenic intracardiac focus
- Choroid plexus cyst
- Renal pyelectasis
- Increased nuchal fold
- Nasal bone absence or hypoplasia
• Advanced Diagnostic Procedures
- NIPT (Non-Invasive Prenatal Testing)
- Amniocentesis
- Chorionic Villus Sampling (CVS)
- Fetal anomaly scans
3. Carrier Screening for Couples Planning Pregnancy
Carrier screening identifies hidden genetic risks in healthy individuals. We screen for:
- Thalassemia
- Sickle cell disease
- Spinal muscular atrophy (SMA)
- Cystic fibrosis
- Other hemoglobinopathies and recessive disorders
Especially recommended for couples with family history, consanguinity, or previous affected child.
4. Genetic Counselling for IVF & High-Risk Pregnancies
Our counsellors work closely with reproductive teams to interpret PGT-A / PGT-M results, assess embryo risks, and guide decisions for IVF/ICSI patients and high-risk pregnancies.
5. Pediatric Genetic Evaluation
We diagnose and manage children with suspected genetic or developmental issues. Areas covered include:
• Developmental & Behavioural Concerns
- Autism spectrum disorder
- Developmental delay
- Learning disabilities, speech delay, behavioral abnormalities
• Growth-Related Issues
- Failure to thrive, short stature
- Early or delayed puberty
• Structural & Physical Abnormalities
- Dysmorphic features, birth defects, organ malformations
• Neuromuscular & Metabolic Concerns
- Floppy infant, recurrent fractures, suspected chromosomal disorders
6. Evaluation for Sudden Unexplained Deaths in the Family
We offer comprehensive family history assessment, genetic risk analysis, and predictive testing to identify hereditary cardiac, metabolic, or neurological conditions and protect at-risk relatives.
7. Thalassemia & Hemoglobinopathy Services
Specialised testing and counselling including trait screening, hemoglobin electrophoresis, genetic confirmation for alpha/beta thalassemia, and family screening.
8. Familial Cancer Genetics & Hereditary Cancer Syndromes
We evaluate patients with family histories suggestive of inherited cancer risk (BRCA1/2, TP53, Lynch genes, etc.), provide testing and counselling, and recommend surveillance and risk-reduction strategies.
9. Genetic Testing & Advanced Diagnostics
- Chromosomal microarray (CMA)
- Karyotyping
- Whole exome sequencing (WES)
- Targeted gene panels & mitochondrial DNA tests
10. Pre-Conception & Family Planning Genetics
Pre-conception counselling for couples planning pregnancy to reduce inherited risk.
11. Metabolic & Rare Disease Evaluation
Assessment for inborn errors of metabolism, neurometabolic disorders, and rare genetic syndromes with early intervention plans.