Fetal Blood Karyotyping: Comprehensive Chromosomal Analysis
Understanding Fetal Blood Karyotyping
Fetal Blood Karyotyping represents a sophisticated genetic diagnostic procedure that provides detailed analysis of fetal chromosomes during pregnancy. This advanced testing method examines the complete chromosomal structure from fetal blood samples, offering invaluable insights into the genetic health of the developing fetus. As a cornerstone of modern prenatal diagnostics, karyotyping helps identify chromosomal abnormalities that could impact fetal development and long-term health outcomes.
What Does Fetal Blood Karyotyping Detect?
This comprehensive genetic test specifically analyzes:
- Chromosomal numerical abnormalities (aneuploidies)
- Structural chromosomal rearrangements
- Specific genetic syndromes including Down syndrome (Trisomy 21)
- Turner syndrome (Monosomy X)
- Klinefelter syndrome (XXY)
- Edwards syndrome (Trisomy 18)
- Patau syndrome (Trisomy 13)
- Chromosomal deletions and duplications
Who Should Consider Fetal Blood Karyotyping?
This test is particularly recommended for:
- Women with abnormal ultrasound findings
- Advanced maternal age (35 years or older)
- Previous pregnancy with chromosomal abnormalities
- Family history of genetic disorders
- Abnormal first or second trimester screening results
- Parents with known chromosomal rearrangements
- Unexplained fetal growth restrictions
Key Benefits of Fetal Blood Karyotyping
- Early Detection: Identifies chromosomal abnormalities before birth
- Comprehensive Analysis: Examines all 46 chromosomes thoroughly
- Accurate Diagnosis: Provides definitive chromosomal information
- Informed Decision Making: Enables better pregnancy management
- Genetic Counseling Support: Expert guidance for result interpretation
- Peace of Mind: Reduces uncertainty about fetal health
Understanding Your Test Results
Your Fetal Blood Karyotyping results will provide detailed information about:
- Normal Results: Indicate typical chromosomal pattern with 46 chromosomes
- Abnormal Results: May show extra, missing, or rearranged chromosomes
- Mosaicism: Presence of two or more cell lines with different chromosomal patterns
- Structural Variations: Changes in chromosome structure without numerical changes
Our genetic counselors provide comprehensive result interpretation and discuss implications for your pregnancy, helping you understand the clinical significance of the findings and available management options.
Test Details and Pricing
| Test Parameter | Details |
|---|---|
| Test Name | Fetal Blood Karyotyping |
| Regular Price | $150 USD |
| Discount Price | $112 USD |
| Turnaround Time | 7-9 days |
| Sample Type | Fetal Blood |
| Test Components | Sodium Heparin Vacutainer (2ml) |
| Methodology | Cell Culture |
Pre-Test Instructions
Fetal Blood Karyotyping requires a doctor’s prescription for proper authorization. Please note that prescriptions are not applicable for surgery and pregnancy cases or individuals planning to travel abroad. Our specialized team ensures proper sample collection and handling to maintain sample integrity throughout the testing process.
Nationwide Accessibility
GGC DNA maintains comprehensive testing facilities across major metropolitan areas throughout the United States. Our strategically located branches in New York, Los Angeles, Chicago, Houston, Phoenix, and other key cities ensure convenient access to advanced genetic testing services. Each facility operates under strict quality control measures and maintains state-of-the-art laboratory equipment.
Take the Next Step Toward Genetic Clarity
Don’t leave your pregnancy questions unanswered. Our expert team of genetic specialists and counselors are ready to guide you through the Fetal Blood Karyotyping process. With rapid 7-9 day turnaround and comprehensive result analysis, we provide the clarity and confidence you need during this important time.
Book your Fetal Blood Karyotyping test today by calling our dedicated genetic counseling line at +1(267) 388-9828 or schedule your appointment online. Take control of your prenatal health with advanced genetic insights from GGC DNA.
