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Microarray 60K AFCVSCB Karyotyping FISH Chromosome 13,18,21,X and Y

Original price was: $1,000.Current price is: $750.

-25%

The Microarray 60K AFCVSCB Karyotyping FISH Chromosome 13,18,21,X and Y test is a comprehensive prenatal genetic screening that combines three advanced technologies to detect chromosomal abnormalities. This sophisticated test analyzes amniotic fluid or chorionic villi samples to identify potential genetic disorders in developing fetuses. It specifically targets chromosomes 13, 18, 21, X, and Y, which are associated with common genetic conditions like Down syndrome, Edwards syndrome, Patau syndrome, and sex chromosome abnormalities. The test provides detailed chromosomal analysis through microarray technology, traditional karyotyping, and FISH methodology for rapid preliminary results. Priced at $750 USD, this advanced screening offers expectant parents crucial information about their baby’s genetic health, enabling informed decisions and appropriate medical planning.

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Microarray 60K AFCVSCB Karyotyping FISH Chromosome 13,18,21,X and Y Test

Comprehensive Prenatal Genetic Screening for Chromosomal Abnormalities

The Microarray 60K AFCVSCB Karyotyping FISH Chromosome 13,18,21,X and Y test represents the gold standard in prenatal genetic screening, combining three powerful diagnostic technologies to provide comprehensive chromosomal analysis. This advanced testing methodology offers expectant parents unparalleled insight into their baby’s genetic health, detecting potential chromosomal abnormalities with exceptional accuracy and precision.

What This Advanced Genetic Test Measures

This comprehensive screening test utilizes multiple analytical approaches to detect chromosomal abnormalities:

  • Microarray 60K Technology: Provides high-resolution analysis of the entire genome, detecting microdeletions and microduplications too small to be seen with traditional methods
  • Karyotyping: Offers complete chromosomal analysis, examining chromosome number, structure, and arrangement
  • FISH (Fluorescence In Situ Hybridization): Delivers rapid preliminary results for chromosomes 13, 18, 21, X, and Y within 24-48 hours

Who Should Consider This Genetic Screening

This comprehensive prenatal test is recommended for:

  • Women with abnormal ultrasound findings suggesting chromosomal abnormalities
  • Pregnancies with advanced maternal age (35 years or older)
  • Previous pregnancy with chromosomal abnormalities
  • Abnormal first or second trimester screening results
  • Family history of genetic disorders or chromosomal conditions
  • Parents carrying balanced chromosomal rearrangements
  • Unexplained fetal growth restriction or structural abnormalities

Clinical Benefits of Comprehensive Prenatal Testing

Choosing this advanced genetic screening provides numerous advantages:

  • Early Detection: Identifies chromosomal abnormalities early in pregnancy, allowing for informed decision-making
  • Comprehensive Analysis: Combines three methodologies for the most thorough chromosomal evaluation available
  • Rapid Preliminary Results: FISH technology provides quick answers for the most common chromosomal conditions
  • High Resolution: Microarray detects subtle genetic changes missed by traditional methods
  • Personalized Care Planning: Enables appropriate medical management and preparation for potential special needs
  • Peace of Mind: Provides reassurance about fetal genetic health or prepares families for specific challenges

Understanding Your Test Results

Your genetic counselor will explain the results in detail, but here’s general guidance:

  • Normal Results: No significant chromosomal abnormalities detected in the analyzed material
  • Abnormal Results: May indicate chromosomal conditions requiring further evaluation and genetic counseling
  • Variants of Uncertain Significance: Some findings may require additional family studies for interpretation
  • Mosaicism: The presence of two or more cell lines with different chromosomal patterns

All abnormal results are confirmed through additional testing and discussed with a certified genetic counselor who provides comprehensive support and guidance.

Test Pricing and Availability

Price Type Amount (USD)
Discount Price $750
Regular Price $1000

Nationwide Accessibility

We have diagnostic centers conveniently located across the United States, including major metropolitan areas such as New York City, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many other cities. Our state-of-the-art facilities ensure consistent, high-quality testing standards nationwide.

Take the Next Step Toward Genetic Clarity

Don’t leave your baby’s genetic health to chance. Our comprehensive prenatal screening provides the detailed information you need for informed pregnancy management. With a turnaround time of 7-9 days and sample collection through amniotic fluid or chorionic villi sampling, this test offers unparalleled genetic insight.

Book your appointment today by calling our genetic counseling team at +1(267) 388-9828 or schedule your consultation online. Take control of your prenatal care with the most advanced genetic screening technology available.

Note: This test requires a doctor’s prescription for most cases, though prescriptions are not applicable for surgical procedures, pregnancy cases, or individuals planning international travel. Our genetic counselors are available to discuss any questions about test preparation, procedure, or results interpretation.