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Parameters

Reports Within:

Parameter Include:

Requisites
Measures

Number of red blood cells in the blood

Identifies

Red blood cell disorders

Measures: Number of red blood cells in the blood

Identifies: Red blood cell disorders

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What is the maximum days the report can be obtained for the test

The maximum days the report can be obtained for the test Karyotyping: Products Of Conception (POC) Reflex Testing To FISH is 14 days.

What are the prerequisites for the test Karyotyping: Products Of Conception (POC) Reflex Testing To FISH

  • Confirmation of pregnancy loss
  • Chromosomal analysis ordered on POC
  • Maternal blood for maternal cell contamination (MCC) testing

What are the measure values for the test Karyotyping: Products Of Conception (POC) Reflex Testing To FISH

  1. Chromosome Analysis - Normal
  2. Chromosome Analysis - Abnormal

What does this test Karyotyping: Products Of Conception (POC) Reflex Testing To FISH identify?

This test, Karyotyping: Products Of Conception (POC) Reflex Testing To FISH, helps identify any genetic abnormalities or chromosomal disorders in the products of conception (POC). Karyotyping involves studying the number, size, and shape of chromosomes in a sample of fetal tissue to detect any abnormalities. The reflex testing to FISH (Fluorescent In Situ Hybridization) is a more specific test that can identify specific chromosomal abnormalities, such as trisomy 21 (Down syndrome), trisomy 18 (Edwards syndrome), or trisomy 13 (Patau syndrome).

Why is this test Karyotyping: Products Of Conception (POC) Reflex Testing To FISH taken?

  • Reason for Test:

    Karyotyping: Products Of Conception (POC) Reflex Testing To FISH is taken to analyze the fetal genetic material from a miscarriage or stillbirth. It helps in determining the cause of pregnancy loss and identifying any chromosomal abnormalities that may have contributed to the event.

  • Procedure:

    The test involves examining the chromosomes of the fetal tissue obtained from the products of conception. Karyotyping is the initial step in this process, where the chromosomes are analyzed for any structural or numerical abnormalities. If the karyotype results are normal or inconclusive, further testing with Fluorescence In Situ Hybridization (FISH) may be performed to detect specific chromosomal abnormalities.

  • Importance:

    Identifying chromosomal abnormalities in the fetal tissue can provide valuable information for understanding the cause of the pregnancy loss and assessing the risk of recurrence in future pregnancies. This information can guide healthcare providers in making informed decisions about genetic counseling, reproductive options, and potential interventions to prevent future losses.

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