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Chromosome Analysis, Blood (Karyotyping)
Original price was: ₹6,000.00.₹4,499.00Current price is: ₹4,499.00.
Turnaround Time (TAT)
10–21 Working Days
Normal Result
- Female: 46,XX
- Male: 46,XY
Clinical Utility
This test detects:
- Numerical chromosomal abnormalities (e.g., trisomy or monosomy)
- Structural abnormalities such as deletions, duplications, translocations, inversions, and marker chromosomes.
Note: Chromosome Analysis (Karyotyping) detects large chromosomal abnormalities. It does not detect small genetic mutations or microdeletions, for which other genetic tests may be required.
Description
Chromosome Analysis, Blood is a genetic test that examines the number and structure of chromosomes in white blood cells from a blood sample. It helps identify chromosomal abnormalities that may cause genetic disorders, infertility, or recurrent pregnancy loss.
Clinical Indications
- Recurrent miscarriages
- Male or female infertility
- Congenital abnormalities
- Developmental delay or intellectual disability
- Suspected chromosomal disorders such as Down syndrome, Turner syndrome, and Klinefelter syndrome
- Selected hematological disorders (when clinically indicated)
Specimen
- 2–5 mL Peripheral Blood
- Collection Tube: Sodium Heparin (Green Top Tube)
Method
- Cell Culture
- G-Banding (Conventional Karyotyping)
- Microscopic Chromosome Analysis
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