Microarray 60K POC Single Karyotyping: Advanced Genetic Analysis for Pregnancy Loss
Comprehensive Introduction to Genetic Testing
The Microarray 60K POC Single Karyotyping test represents a cutting-edge approach to genetic analysis, combining the precision of microarray technology with the established reliability of traditional karyotyping. This comprehensive diagnostic tool is specifically designed to investigate chromosomal abnormalities in products of conception, providing crucial insights for couples experiencing pregnancy loss. By utilizing advanced Agilent microarray technology capable of analyzing over 60,000 genetic markers, this test offers unprecedented resolution in detecting subtle genetic variations that may contribute to reproductive challenges.
What This Advanced Test Detects
The Microarray 60K POC Single Karyotyping test provides comprehensive analysis of chromosomal structure and content, detecting:
- Chromosomal aneuploidies (abnormal chromosome numbers)
- Microdeletions and microduplications too small for conventional karyotyping
- Unbalanced chromosomal rearrangements
- Regions of homozygosity that may indicate consanguinity
- Subtelomeric imbalances often missed by standard testing
- Mosaicism in chromosomal composition
Clinical Applications and Detection Capabilities
This advanced genetic test can identify numerous genetic conditions including Down syndrome, Turner syndrome, Klinefelter syndrome, and various microdeletion syndromes such as DiGeorge syndrome and Williams syndrome. The high-resolution microarray component detects copy number variations as small as 50-100 kilobases, providing detailed genetic information beyond what traditional methods can reveal.
Who Should Consider This Genetic Test
This comprehensive genetic analysis is particularly recommended for:
- Couples experiencing recurrent pregnancy loss
- Women with unexplained fetal demise
- Patients with abnormal ultrasound findings in previous pregnancies
- Couples with family history of chromosomal abnormalities
- Women of advanced maternal age (35 years and older)
- Cases where standard karyotyping yielded normal results but clinical suspicion remains
- Couples planning future pregnancies after previous genetic concerns
Symptoms and Clinical Indicators
Consider this test if you’ve experienced:
- Multiple miscarriages without clear cause
- Stillbirth or intrauterine fetal demise
- Previous pregnancy with chromosomal abnormalities
- Family history of genetic disorders
- Unexplained infertility issues
- Advanced paternal age concerns
Significant Benefits of Comprehensive Genetic Testing
Choosing the Microarray 60K POC Single Karyotyping test provides numerous advantages:
- Enhanced Diagnostic Yield: Detects up to 10-15% more abnormalities compared to conventional karyotyping alone
- Comprehensive Analysis: Combines the strengths of both microarray and traditional methods
- Future Pregnancy Planning: Provides valuable information for genetic counseling and reproductive decisions
- Emotional Closure: Helps couples understand the reasons behind pregnancy loss
- Cost-Effective: Comprehensive testing at a fraction of the cost of separate procedures
- Quick Results: Turnaround time of just 7-9 days for timely decision-making
Understanding Your Test Results
Your genetic test results will be carefully interpreted by our expert genetic counselors and medical professionals:
Normal Results Interpretation
A normal result indicates no detectable chromosomal abnormalities in the analyzed sample. This can provide reassurance and help narrow down other potential causes of pregnancy loss. However, it’s important to understand that genetic testing cannot detect all possible genetic conditions.
Abnormal Findings Guidance
If abnormalities are detected, our genetic counseling team will:
- Explain the specific genetic findings in understandable terms
- Discuss the clinical significance of the detected abnormalities
- Provide information about recurrence risks for future pregnancies
- Offer guidance on available reproductive options
- Connect you with appropriate medical specialists if needed
Variants of Uncertain Significance
Some genetic variations may be classified as variants of uncertain significance (VUS). Our team will explain what this means and discuss any recommended follow-up testing or family studies that might help clarify the finding.
Test Pricing and Appointment Information
| Test Component | Price (USD) |
|---|---|
| Discount Price | $376 |
| Regular Price | $500 |
| Test Name | Microarray 60K POC Single Karyotyping |
Sample Requirements and Processing
This test requires products of conception samples collected in sterile containers with normal saline. Peripheral blood samples from parents may also be recommended for comparative analysis. The test utilizes advanced microarray technology from Agilent combined with cell culture methods for comprehensive chromosomal assessment.
Nationwide Availability and Booking
We have diagnostic centers conveniently located across the United States, including major metropolitan areas such as New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our state-of-the-art facilities ensure consistent, high-quality testing standards nationwide.
Pre-Test Instructions
The Microarray 60K POC Single Karyotyping test requires a doctor’s prescription in most cases. However, prescription requirements do not apply for surgical cases, pregnancy-related testing, or individuals planning international travel. Our team will guide you through the specific requirements based on your situation.
Take the Next Step Toward Understanding
Don’t let unanswered questions about pregnancy loss continue to affect your family planning decisions. Our compassionate team of genetic specialists is ready to provide the comprehensive analysis and support you need.
Call us today at +1(267) 388-9828 to schedule your appointment or speak with our genetic counseling team. We’re here to help you find answers and move forward with confidence.
With a quick 7-9 day turnaround time and our network of locations across the country, getting the genetic information you need has never been more accessible. Take control of your reproductive health journey today.
