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Chromosome Analysis Test

Report Delivery Time: 3 Days

Recommended Gender: Both

Sample Type: Blood

The Chromosome Analysis Test, also known as a karyotyping test, is a genetic test that identifies chromosomal abnormalities. It is crucial in diagnosing genetic disorders, infertility issues, developmental delays, and blood cancers.

4,000.00

Whatsapp

+919354028488

Email Address

info@hprimelabs.com

Email Address

customercare@hprimelabs.com

4,000.00

Whatsapp

+919354028488

Email Address

info@hprimelabs.com

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What is the Chromosome Analysis Test?

The Chromosome Analysis Test—also called a karyotyping test—examines a person’s chromosomes in terms of number and structure. This diagnostic test helps detect conditions like Down syndrome, Turner syndrome, Klinefelter syndrome, and supports fertility evaluations and cancer diagnosis.

Doctors often recommend the Chromosome Analysis Test to evaluate causes of miscarriages, infertility, or developmental problems. It plays a critical role in both prenatal screening and cancer monitoring.

Note: This test is not used to detect individual gene mutations but large-scale chromosomal issues.


Parameters Covered

  • Chromosome Number and Structure – Detects numerical or structural abnormalities

  • Chromosomal Rearrangements – Identifies duplications, deletions, inversions, or translocations

  • Karyotype Imaging – Generates a full image of the 23 pairs of chromosomes for evaluation


Why is the This Test Important?

  • Detects genetic causes of miscarriage or infertility

  • Diagnoses chromosomal disorders such as Down syndrome

  • Aids in prenatal diagnosis of inherited abnormalities

  • Evaluates cancer-related chromosomal changes in leukemia and lymphoma

  • Provides crucial information for reproductive health decisions


Who Should Take This Test?

  • Couples with repeated miscarriages or infertility

  • Children with birth defects or developmental delays

  • Pregnant women undergoing prenatal screening

  • Cancer patients, especially leukemia or lymphoma

  • Individuals with family history of genetic disorders


Test Procedure and Preparation

  • Sample Type: Blood (most common), bone marrow, or amniotic fluid (prenatal)

  • Fasting: Not required

  • Test Duration: Results take 7 to 14 days due to detailed chromosome mapping

  • Preparation: None required unless advised by your doctor


Understanding the Results

Normal results will show 46 chromosomes (23 pairs). Abnormal results might include missing or extra chromosomes, such as Trisomy 21 in Down syndrome, or structural issues. Results from your Chromosome Analysis Test or karyotyping test will be interpreted by a geneticist or physician.

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