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Chromosome Analysis Test

Report Delivery Time: 3 Days

Recommended Gender: Both

Sample Type: Blood

The Chromosome Analysis Test (Karyotyping) examines a person’s chromosomes to detect genetic abnormalities, chromosomal disorders, and structural changes. It is commonly used for diagnosing genetic disorders, infertility causes, recurrent miscarriages, and certain 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

Related Packages

Related Tets

The Chromosome Analysis (Karyotyping) Test is a laboratory test that examines the number, shape, and structure of chromosomes in a person’s cells. Chromosomes contain genetic information, and any abnormalities may cause birth defects, genetic disorders, infertility, or blood cancers.

Why is the Test Done?

This test is used for:

Detecting chromosomal abnormalities – Identifies genetic disorders like Down syndrome, Turner syndrome, and Klinefelter syndrome.
Infertility assessment – Helps find chromosomal reasons behind infertility and recurrent miscarriages.
Prenatal testing – Checks for genetic abnormalities in a developing baby.
Cancer diagnosis – Identifies chromosomal changes linked to leukemia, lymphoma, and other blood disorders.
Developmental disorders – Helps diagnose children with intellectual disabilities, developmental delays, or birth defects.

Who Should Get This Test?

This test is recommended for:

Couples experiencing repeated miscarriages or infertility.
Pregnant women undergoing prenatal genetic screening.
Individuals with a family history of genetic disorders.
Children with unexplained developmental delays or birth defects.
People diagnosed with leukemia or lymphoma for treatment planning.

Test Procedure & Preparation

Preparation:

  • No special preparation is needed.
  • Inform your doctor about any medications.

Procedure:

  • A blood sample (or sometimes bone marrow or amniotic fluid for prenatal testing) is collected.
  • The sample is analyzed in a laboratory to examine the chromosomes under a microscope.
  • The test results help identify chromosomal abnormalities or mutations.

Understanding the Results

  • Normal Results: 46 chromosomes (23 pairs) with no structural changes.
  • Abnormal Results: May indicate missing, extra, or rearranged chromosomes, leading to genetic conditions such as:
    • Down Syndrome (Trisomy 21) – An extra chromosome 21.
    • Turner Syndrome (45, X) – A missing X chromosome in females.
    • Klinefelter Syndrome (47, XXY) – An extra X chromosome in males.
    • Leukemia-associated abnormalities – Changes in chromosomes linked to blood cancers.

Limitations of the Test

Cannot detect single-gene mutations – Used only for large chromosomal abnormalities.
Not a direct diagnostic test for diseases – Further genetic tests may be required.
Results take time – Karyotyping analysis may take 1-3 weeks.

Why is the Chromosome Analysis Test Important?

Essential for diagnosing genetic disorders and infertility.
Helps in prenatal genetic screening for birth defects.
Aids in diagnosing and managing blood cancers.

This test plays a crucial role in genetic counseling, pregnancy planning, and cancer diagnosis, providing valuable insights into chromosomal health.

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