Karyotyping by G-Banding, Peripheral Blood in Taloja
51+ booked in last 3 daysKaryotyping Test Overview
A karyotype test looks at the size, shape, and number of your chromosomes.
Karyotyping by G-Banding, Peripheral Blood Price in Taloja
Metropolis Healthcare is a leading diagnostics centre and pathology lab in India equipped with the latest state-of-the-art technologies that provides the Karyotyping by G-Banding, Peripheral Blood with a clear pricing structure
The price of Karyotyping by G-Banding, Peripheral Blood in Taloja is ₹ 4,300
We are committed to deliver accurate and quality results from the best labs in India with complete transparency regarding test cost and turnaround time. No matter where you are, we strive to offer patients high-quality service that is affordable and accessible.
Frequently Asked Questions
To find chromosome abnormalities, in order to help diagnose genetic diseases, any birth defects, and some disorders of the blood and lymphatic system.
Your doctor would recommend this test if
- The foetus is suspected of having a chromosomal abnormality,
- If an infant has congenital abnormalities,
- If a woman has been experiencing miscarriages or infertility,
- When an adult shows signs of a genetic disorder.
Chromosome examination or karyotyping is a test that study the number and shape of a person's chromosomes in order to find abnormalities. Chromosomes are thread-like structures inside each cell nucleus and contain the body's genetic plan. Each chromosome contains thousands of genes in certain locations. These genes are responsible for a person’s congenital physical characteristics and they have a significant impact on growth, development, and functioning of the body.
Humans have 46 chromosomes, present as 23 pairs. 22 pairs are found in both sexes (autosomes) and one pair (sex chromosomes) is present as either XY (in males) or XX (in females). Normally, all cells in the body that have a nucleus will comprise a complete set of the same 46 chromosomes, except for the reproductive cells (eggs and sperm), which contain a half set of 23. This half set is the genetic contribution that will be passed on to a child. At conception, half sets from each parent combine to form a new set of 46 chromosomes in the developing foetus.
A chromosomal karyotyping examines a person's chromosomes to verify if the right number is present and to ascertain if each chromosome appears normal.
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