Chromosomes 13 and 21 Analysis: Comprehensive Genetic Screening
Understanding Chromosomes 13 & 21 Analysis
The Chromosomes 13 and 21 Analysis represents a cutting-edge genetic testing approach that specifically targets two critical chromosomes associated with significant genetic disorders. Using Fluorescence In Situ Hybridization (FISH) technology, this test provides rapid and accurate detection of chromosomal abnormalities that can impact fetal development and overall health outcomes.
What This Test Measures and Detects
This specialized genetic analysis focuses on identifying:
- Trisomy 21 (Down syndrome) – extra copy of chromosome 21
- Trisomy 13 (Patau syndrome) – extra copy of chromosome 13
- Chromosomal translocations involving chromosomes 13 and 21
- Deletions or duplications in specific chromosomal regions
- Mosaicism patterns in chromosomal distribution
Who Should Consider Chromosomes 13 & 21 Testing?
This genetic screening is particularly recommended for:
- Pregnant women with abnormal ultrasound findings
- Individuals with family history of chromosomal disorders
- Advanced maternal age (35 years and older)
- Abnormal first-trimester or second-trimester screening results
- Previous pregnancy with chromosomal abnormalities
- Couples with recurrent pregnancy loss
- Individuals planning family with known genetic risks
Clinical Indications and Symptoms
The test is indicated when there are concerns about:
- Fetal growth abnormalities detected during ultrasound
- Increased nuchal translucency measurements
- Multiple congenital anomalies suspected
- Developmental delays or intellectual disabilities
- Family history of genetic syndromes
- Advanced paternal age considerations
Benefits of Chromosomes 13 & 21 Analysis
Choosing this advanced genetic testing provides numerous advantages:
- Early Detection – Identify chromosomal abnormalities before birth
- Rapid Results – Receive comprehensive findings within 3-4 days
- High Accuracy – FISH technology provides precise chromosomal analysis
- Informed Decision Making – Empower families with crucial genetic information
- Comprehensive Screening – Target specific high-risk chromosomal regions
- Minimal Risk – Non-invasive sample collection procedures
Sample Collection and Processing
Our testing utilizes specialized sample types including:
- Amniotic fluid collected during amniocentesis
- Chorionic villi samples from CVS procedures
- Cord blood specimens when indicated
All samples are processed using sterile containers, normal saline solutions, and sodium heparin vacutainers to ensure sample integrity and accurate results.
Understanding Your Test Results
Your Chromosomes 13 and 21 Analysis results will provide clear information about:
- Normal Results – Indicate typical chromosomal patterns with no detected abnormalities
- Abnormal Findings – Identify specific chromosomal variations requiring further evaluation
- Mosaic Patterns – Show mixed cell populations with different chromosomal compositions
- Clinical Significance – Detailed explanation of how findings may impact health outcomes
All positive results are accompanied by genetic counseling recommendations to help you understand the implications and next steps. Our team provides comprehensive support throughout the interpretation process.
Test Pricing and Availability
| Price Type | Amount (USD) |
|---|---|
| Discount Price | $150 |
| Regular Price | $200 |
Nationwide Accessibility
We have established branches across major cities in the United States, ensuring convenient access to our advanced genetic testing services. Our facilities are located in:
- New York City, NY
- Los Angeles, CA
- Chicago, IL
- Houston, TX
- Phoenix, AZ
- Philadelphia, PA
- San Antonio, TX
- San Diego, CA
- Dallas, TX
- San Jose, CA
Book Your Chromosomes 13 & 21 Analysis Today
Take the first step toward comprehensive genetic screening and peace of mind. Our experienced genetic counselors and laboratory specialists are ready to assist you with:
- Professional sample collection
- Accurate FISH analysis
- Comprehensive result interpretation
- Genetic counseling support
- Follow-up care coordination
Call or WhatsApp us today at +1(267) 388-9828 to schedule your appointment or discuss your genetic testing needs with our specialists.
Note: Chromosomes 13 & 21 Analysis requires a doctor’s prescription for most cases. Prescription requirements may not apply for surgery, pregnancy-related cases, or individuals planning international travel. Consult with our genetic counselors for specific requirements based on your situation.
