Chromosome Analysis (Karyotyping) Peripheral Blood

    Chromosome Analysis (Karyotyping) Peripheral Blood

    Chromosome analysis, or karyotyping, is a genetic test that examines the number and structure of chromosomes in a sample of whole blood. This test measures various health markers that can indicate genetic disorders or abnormalities. It is essential for diagnosing conditions related to chromosomal abnormalities.

    Quick Summary

    Chromosome Analysis (Karyotyping) Peripheral Blood Price AED 1500, Sample 5 mL (3 mL min.) Whole blood in 2 Green Top (Sodium Heparin) tubes. Ship refrigerated immediately. DO NOT FREEZE. Genomic TRF, Informed Consent and Clinical history is mandatory,, Results in 10 - 12 Days. Home collection available.

    Test Overview

    Result Time

    10 - 12 Days

    Sample Type

    5 mL (3 mL min.) Whole blood in 2 Green Top (Sodium Heparin) tubes. Ship refrigerated immediately. DO NOT FREEZE. Genomic TRF, Informed Consent and Clinical history is mandatory,

    Category

    Genetic Testing

    How to Prepare

    To prepare for this test, collect 5 mL (minimum 3 mL) of whole blood in 2 Green Top (Sodium Heparin) tubes. Ensure that the samples are shipped refrigerated immediately. DO NOT FREEZE. A genomic test requisition form, informed consent, and clinical history are mandatory.

    Why You Need This Test

    This test is crucial for identifying genetic disorders and chromosomal abnormalities that can affect health and development. It is often recommended for individuals with unexplained developmental delays, infertility, or recurrent miscarriages. Early detection can lead to better management of potential health issues.

    Clinical Significance

    Karyotyping is essential for diagnosing genetic disorders and understanding chromosomal abnormalities.

    At a Glance

    Quick Facts

    • • Price AED 1500
    • • Sample 5 mL (3 mL min.) Whole blood in 2 Green Top (Sodium Heparin) tubes. Ship refrigerated immediately. DO NOT FREEZE. Genomic TRF, Informed Consent and Clinical history is mandatory,
    • • Results in 10 - 12 Days
    • • Fasting Not required

    What It Measures

    Chromosome analysis, or karyotyping, is a genetic test that examines the number and structure of chromosomes in a sample...

    Frequently Asked Questions

    What does this test measure?

    This test measures the number and structure of chromosomes in the blood sample, which can help identify genetic disorders or abnormalities. It provides insights into potential health risks related to chromosomal changes.

    Who should take this test?

    Individuals experiencing unexplained developmental delays, infertility, or recurrent miscarriages should consider this test. It is also recommended for those with a family history of genetic disorders.

    How do I prepare for this test?

    Prepare by collecting 5 mL (minimum 3 mL) of whole blood in 2 Green Top (Sodium Heparin) tubes. Ensure the samples are shipped refrigerated immediately. DO NOT FREEZE. A genomic test requisition form, informed consent, and clinical history are required.

    What do the results mean?

    Results indicate whether the chromosomes are normal or if there are any abnormalities present. Abnormal results may suggest genetic disorders that require further investigation or management.

    How long until I get my results?

    The turnaround time for results is typically 10 to 12 days. Results will be delivered through the specified communication method.

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    Chromosome Analysis (Karyotyping) Peripheral Blood

    AED 1500
    professional_lab_test

    result_time

    10 - 12 Days

    sample_type

    5 mL (3 mL min.) Whole blood in 2 Green Top (Sodium Heparin) tubes. Ship refrigerated immediately. DO NOT FREEZE. Genomic TRF, Informed Consent and Clinical history is mandatory,

    category

    Genetic Testing

    ✓ certified_lab

    ✓ accurate_results

    ✓ home_collection_available

    ✓ digital_report