Microarray 60K Peripheral Blood Cord Blood Fetal Blood Karyotyping
Comprehensive Introduction to Advanced Genetic Analysis
The Microarray 60K + Karyotyping test represents the gold standard in chromosomal analysis, combining cutting-edge microarray technology with traditional karyotyping methods. This comprehensive approach provides unparalleled accuracy in detecting genetic abnormalities that could impact health, development, and overall wellbeing. As one of the most sophisticated genetic screening tools available, this test offers healthcare providers and patients detailed insights into chromosomal structure and genetic variations.
Genetic testing has revolutionized modern medicine, and the Microarray 60K + Karyotyping combination stands at the forefront of this advancement. By integrating two powerful methodologies, this test delivers comprehensive chromosomal evaluation that single-method tests cannot match. The importance of this testing lies in its ability to detect both large-scale chromosomal abnormalities and subtle genetic variations that might otherwise go undetected.
What This Advanced Genetic Test Measures and Detects
The Microarray 60K + Karyotyping test provides comprehensive analysis of chromosomal structure and genetic material through dual methodology:
Microarray 60K Analysis
- Detects microdeletions and microduplications as small as 50-100 kilobases
- Identifies copy number variations (CNVs) across the entire genome
- Analyzes over 60,000 genetic markers simultaneously
- Provides high-resolution mapping of chromosomal regions
- Detects submicroscopic abnormalities invisible to conventional methods
Traditional Karyotyping
- Visualizes entire chromosome structure and number
- Detects large-scale chromosomal abnormalities
- Identifies translocations, inversions, and aneuploidies
- Provides confirmation of microarray findings
- Offers complementary information about chromosomal organization
Who Should Consider This Comprehensive Genetic Testing
This advanced genetic analysis is recommended for individuals and families in various clinical scenarios:
Prenatal and Pregnancy Cases
- Advanced maternal age (35 years or older)
- Abnormal ultrasound findings
- Family history of genetic disorders
- Previous pregnancy with chromosomal abnormalities
- Unexplained recurrent pregnancy loss
Pediatric and Developmental Concerns
- Children with developmental delays
- Multiple congenital anomalies
- Intellectual disability of unknown cause
- Autism spectrum disorders
- Growth abnormalities and failure to thrive
Adult Genetic Screening
- Unexplained infertility issues
- Family planning and preconception screening
- Suspected genetic syndromes
- Recurrent miscarriages
- Genetic counseling requirements
Significant Benefits of Comprehensive Chromosomal Analysis
Choosing the Microarray 60K + Karyotyping test provides numerous advantages for patients and healthcare providers:
Enhanced Diagnostic Accuracy
The combination of microarray and karyotyping technologies offers complementary benefits that significantly improve diagnostic accuracy. While microarray detects subtle genetic variations, karyotyping confirms larger structural abnormalities, creating a comprehensive diagnostic picture.
Early Intervention Opportunities
Early detection of genetic abnormalities enables timely medical interventions, specialized care planning, and informed family decisions. This proactive approach can significantly improve outcomes and quality of life.
Comprehensive Risk Assessment
This test provides complete chromosomal evaluation, offering peace of mind through thorough genetic screening. The dual-methodology approach ensures no significant abnormalities are missed, providing reliable results for critical healthcare decisions.
Family Planning Guidance
For couples planning pregnancy or experiencing fertility challenges, this test offers valuable genetic information that can guide reproductive decisions and family planning strategies.
Understanding Your Genetic Test Results
Receiving and interpreting genetic test results requires professional medical guidance. Here’s general information about potential outcomes:
Normal Results
A normal result indicates no significant chromosomal abnormalities were detected using both microarray and karyotyping methods. This provides reassurance about chromosomal health but doesn’t guarantee absence of all genetic conditions.
Abnormal Findings
Abnormal results may indicate various genetic conditions, including chromosomal disorders, microdeletion syndromes, or copy number variations. All abnormal findings require consultation with a genetic counselor or specialist for proper interpretation and management planning.
Variants of Uncertain Significance
Some genetic variations may be classified as variants of uncertain significance (VUS). These findings require careful consideration and may need additional family studies or follow-up testing for proper interpretation.
Clinical Correlation
All genetic test results must be interpreted in the context of clinical symptoms, family history, and other medical findings. Your healthcare provider will help you understand how the results relate to your specific health situation.
Test Information and Pricing
| Test Component | Details |
|---|---|
| Test Name | Microarray 60K Peripheral Blood Cord Blood Fetal Blood Karyotyping |
| Regular Price | $750 USD |
| Discount Price | $562 USD |
| Turnaround Time | 7-9 Days |
| Sample Type | Peripheral Blood |
| Test Components | EDTA & Heparinised Vacutainer (3 ml each) |
| Methodology | Microarray [Agilent] + Cell Culture |
Pre-Test Instructions and Requirements
The Microarray 60K (Peripheral Blood/Cord Blood/Fetal Blood) + Karyotyping test requires a Doctor’s prescription for most cases. However, prescription requirements do not apply for surgery preparation, pregnancy cases, or individuals planning international travel. Our genetic counseling team can provide guidance on test appropriateness and help coordinate necessary documentation.
Nationwide Accessibility Across the United States
We proudly serve patients across all major metropolitan areas in the United States, with convenient testing locations in:
- New York City and surrounding regions
- Los Angeles and Southern California
- Chicago and Illinois metropolitan area
- Houston and Texas Gulf Coast
- Phoenix and Arizona communities
- Philadelphia and Pennsylvania region
- San Antonio and South Texas
- San Diego and California coast
- Dallas and North Texas area
- San Jose and Silicon Valley
Take the Next Step Toward Genetic Clarity
Understanding your genetic health is one of the most important steps you can take for comprehensive healthcare planning. Our Microarray 60K + Karyotyping test provides the detailed chromosomal analysis needed for informed medical decisions and peace of mind.
Ready to schedule your genetic testing? Contact our genetic specialists today to discuss your testing needs, insurance coverage, and appointment availability. Call us at +1(267) 388-9828 or book your consultation online through our secure patient portal.
Our dedicated team of genetic counselors and medical professionals is committed to providing compassionate care and comprehensive support throughout your testing journey. We understand that genetic testing can raise important questions, and we’re here to provide the answers and guidance you need.
