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Karyotyping — Chromosomal Analysis
Understand your genes. Plan a better tomorrow.
Karyotyping is a laboratory test that analyzes the number, structure and appearance of chromosomes in a sample of cells. It helps detect genetic disorders, chromosomal abnormalities and congenital conditions. Turnaround: 7–10 working days.
Home Sample Collection Trusted Diagnostics Fast Reports Expert Doctors
PRICE
₹8400
₹12000
All inclusive · Home collection available
Reports on WhatsApp / Email
Sterile, hygienic process
7 days a week service
Package Includes
- Numerical Abnormalities (Down, Turner, Klinefelter Syndrome)
- Structural Abnormalities (Deletions, Duplications, Translocations, Inversions)
- Congenital Abnormalities evaluation
- Recurrent Pregnancy Loss investigation
- Developmental Disorders screening
- Sample types: Blood / Bone Marrow / Amniotic Fluid / Other Tissues
Ideal For
- Couples with recurrent pregnancy loss or infertility
- Pregnant women with abnormal ultrasound findings
- Newborns with congenital anomalies
- Individuals with developmental delay or intellectual disability
- Family history of genetic or chromosomal disorders
Why this package
Accurate & Reliable Results
Detailed chromosomal analysis by experts.
Detects a Wide Range of Disorders
Numerical, structural & congenital.
Guides Reproductive Decisions
Helpful for couples & expecting parents.
Supports Early Intervention
Diagnosis enables timely care planning.
Expert Genetic Counseling
Personalized support every step of the way.