Prenatal Diagnostic Screening by Karyotyping FISH for Chromosomes 13, 18, 21, X and Y
Comprehensive Chromosomal Analysis for Prenatal Health
Our Prenatal Diagnostic Screening represents the gold standard in chromosomal analysis, combining traditional karyotyping with advanced Fluorescence In Situ Hybridization (FISH) technology. This powerful diagnostic approach provides definitive information about your baby’s chromosomal health, specifically targeting the most common and clinically significant chromosomal abnormalities that can affect fetal development.
What This Advanced Test Measures and Detects
This comprehensive screening test specifically analyzes five critical chromosomal regions:
- Chromosome 21: Detection of Down syndrome (trisomy 21)
- Chromosome 18: Identification of Edwards syndrome (trisomy 18)
- Chromosome 13: Screening for Patau syndrome (trisomy 13)
- Sex Chromosomes X and Y: Analysis of sex chromosome abnormalities including Turner syndrome, Klinefelter syndrome, and other sex chromosome variations
Who Should Consider This Prenatal Diagnostic Test
This advanced screening is particularly recommended for:
- Women with abnormal first or second trimester screening results
- Advanced maternal age (35 years or older)
- Previous pregnancy with chromosomal abnormalities
- Family history of genetic disorders
- Abnormal ultrasound findings
- Parents carrying balanced chromosomal rearrangements
Significant Benefits of Comprehensive Prenatal Screening
- Early Detection: Identify chromosomal abnormalities weeks before birth
- Accurate Diagnosis: Combined Karyotyping and FISH provide complementary confirmation
- Informed Decision Making: Essential information for pregnancy management
- Peace of Mind: Reduce uncertainty about fetal chromosomal health
- Comprehensive Analysis: Covers the most common clinically significant chromosomal disorders
Understanding Your Test Results
Your results will provide clear chromosomal analysis:
- Normal Results: Indicate typical chromosomal patterns for the tested chromosomes
- Abnormal Results: Identify specific chromosomal abnormalities with detailed explanations
- Genetic Counseling: Comprehensive consultation available to discuss results and implications
- Follow-up Guidance: Clear recommendations for next steps based on findings
Test Details and Pricing
| Test Feature | Details |
|---|---|
| Test Name | Prenatal Diagnostic Screening by Karyotyping FISH for Chromosomes 13, 18, 21, X and Y |
| Discount Price | $450 USD |
| Regular Price | $600 USD |
| Turnaround Time | 15-20 days |
| Sample Type | Amniotic fluid / Bits of Chorionic tissue |
| Test Components | 2 sterile tubes (15 ml each) / Sterile tissue culture container with normal saline or culture media |
Nationwide Accessibility
We proudly serve patients across the United States with convenient locations in major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our network of certified genetic testing facilities ensures consistent, high-quality results nationwide.
Take the Next Step in Prenatal Care
Don’t leave your baby’s chromosomal health to chance. Our advanced Prenatal Diagnostic Screening provides the definitive answers you need for informed pregnancy decisions. With our current special pricing of $450 USD (regularly $600 USD), now is the perfect time to ensure comprehensive chromosomal analysis.
Call or WhatsApp us today at +1(267) 388-9828 to schedule your appointment or speak with our genetic counseling team. Our specialists are ready to guide you through the testing process and answer all your questions about prenatal chromosomal screening.
