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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

Maximum Days for QF-PCR + MCC Tests

The report for the test QF-PCR (T13, T18, T21, X & Y) + MCC Tests can be obtained within 7-10 business days from the date of sample collection.

What are the prerequisites for the test QF-PCR (T13,T18,T21, X & Y) + MCC Tests

  • Maternal blood sample
  • Ultrasound reports
  • Previous test results, if any
  • Consent form signed by the patient
  • Referral from a healthcare provider

What are the measure values for the test QF-PCR (T13,T18,T21, X & Y) + MCC Tests

Test Measure Values
QF-PCR (T13) 99.8% sensitivity, 99.7% specificity
QF-PCR (T18) 99.9% sensitivity, 99.9% specificity
QF-PCR (T21) 99.7% sensitivity, 99.8% specificity
QF-PCR (X) 99.6% sensitivity, 99.5% specificity
QF-PCR (Y) 99.4% sensitivity, 99.6% specificity
MCC Tests Specific values may vary depending on the specific test within the MCC category

What does this test QF-PCR (T13,T18,T21, X & Y) + MCC Tests identify?

  • Test Name: QF-PCR (T13, T18, T21, X & Y) + MCC Tests
  • Identifies: This test is used to identify common chromosomal abnormalities such as Trisomy 13 (T13), Trisomy 18 (T18), Trisomy 21 (T21), as well as abnormalities in the sex chromosomes X and Y. These abnormalities can result in genetic disorders and developmental delays.

Why is this test QF-PCR (T13,T18,T21, X & Y) + MCC Tests taken?

Reasons for taking QF-PCR + MCC Tests

QF-PCR (Quantitative Fluorescent Polymerase Chain Reaction) is a genetic test used to detect common chromosomal abnormalities, including Trisomy 13 (T13), Trisomy 18 (T18), and Trisomy 21 (T21), as well as abnormalities in the sex chromosomes X and Y. MCC (Multiplex Ligation-dependent Probe Amplification) is another genetic test that can provide additional information about chromosomal abnormalities.

These tests are often taken during pregnancy to screen for genetic conditions that may affect the health of the baby. Common reasons for taking these tests include:

  • Screening for chromosomal abnormalities such as Down syndrome (T21), Edwards syndrome (T18), and Patau syndrome (T13) which can impact the baby's development and health.
  • Determining the sex of the baby and detecting any abnormalities in the sex chromosomes X and Y.
  • Providing information to parents and healthcare providers about the baby's genetic makeup to help make informed decisions about pregnancy management and care.
  • Identifying potential genetic conditions early in pregnancy to allow for additional testing or interventions if needed.

Overall, QF-PCR + MCC tests are important tools in prenatal care to assess the genetic health of the baby and provide valuable information to parents and healthcare providers.

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