DMD Mutation Screening (79 Exons) [Prenatal]

    DMD Mutation Screening (79 Exons) [Prenatal]

    DMD mutation screening is a prenatal test that analyzes the 79 exons of the DMD gene to identify potential mutations associated with Duchenne Muscular Dystrophy. This test is crucial for assessing the risk of the condition in the fetus, providing valuable information for expectant parents.

    Quick Summary

    DMD Mutation Screening (79 Exons) [Prenatal] Price AED 2000, Sample Amniotic fluid/ Chorionic villi/ Cord Blood +2ml EDTA blood of mother for MCC, Results in 15-20 DAYS. Fasting. Home collection available.

    Test Overview

    Result Time

    15-20 DAYS

    Sample Type

    Amniotic fluid/ Chorionic villi/ Cord Blood +2ml EDTA blood of mother for MCC

    Category

    Genetic Testing

    How to Prepare

    For this test, amniotic fluid, chorionic villi, or cord blood specimens are required, along with 2ml of EDTA blood from the mother for maternal cell contamination (MCC) analysis. No fasting is required, but it is essential to follow any specific instructions provided by your healthcare provider regarding medication or other preparations.

    Why You Need This Test

    This test is significant for expectant parents who may have a family history of Duchenne Muscular Dystrophy or related conditions. It helps detect genetic mutations early, allowing for informed decision-making regarding the pregnancy and potential interventions.

    Clinical Significance

    This test plays a critical role in prenatal genetic screening for Duchenne Muscular Dystrophy.

    At a Glance

    Quick Facts

    • • Price AED 2000
    • • Sample Amniotic fluid/ Chorionic villi/ Cord Blood +2ml EDTA blood of mother for MCC
    • • Results in 15-20 DAYS
    • • Fasting Required

    What It Measures

    DMD mutation screening is a prenatal test that analyzes the 79 exons of the DMD gene to identify potential mutations ass...

    Frequently Asked Questions

    What does this test measure?

    This test measures mutations in the DMD gene, specifically analyzing 79 exons to identify any genetic changes that may lead to Duchenne Muscular Dystrophy. Understanding these mutations helps assess the risk of the condition in the fetus.

    Who should take this test?

    This test is recommended for pregnant individuals with a family history of Duchenne Muscular Dystrophy or those who have had abnormal screening results. It is also useful for couples who are carriers of DMD mutations.

    How do I prepare for this test?

    Preparation for this test involves providing amniotic fluid, chorionic villi, or cord blood samples, along with 2ml of EDTA blood from the mother. No fasting is necessary, but follow any specific instructions from your healthcare provider.

    What do the results mean?

    Results from this test can indicate the presence or absence of mutations in the DMD gene. Abnormal results may suggest a higher risk of Duchenne Muscular Dystrophy in the fetus, prompting further counseling and testing.

    How long until I get my results?

    The turnaround time for this test is typically 15-20 days. Results will be communicated through your healthcare provider, ensuring you receive timely information.

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    DMD Mutation Screening (79 Exons) [Prenatal]

    AED 2000
    professional_lab_test

    result_time

    15-20 DAYS

    sample_type

    Amniotic fluid/ Chorionic villi/ Cord Blood +2ml EDTA blood of mother for MCC

    category

    Genetic Testing

    ✓ certified_lab

    ✓ accurate_results

    ✓ home_collection_available

    ✓ digital_report