Chromosomes 13, 18, 21, X, Y Analysis
Comprehensive Genetic Screening for Chromosomal Abnormalities
The Chromosomes 13, 18, 21, X, Y Analysis represents a cutting-edge approach to genetic screening that provides detailed insights into chromosomal health and integrity. This specialized test employs Fluorescence In Situ Hybridization (FISH) technology to examine five critical chromosomes that are most commonly associated with significant genetic disorders. By focusing on these specific chromosomes, healthcare providers can obtain rapid, accurate information about potential chromosomal abnormalities that could impact development and health outcomes.
What This Advanced Genetic Test Measures
Our Chromosomes 13, 18, 21, X, Y Analysis specifically targets and evaluates:
- Chromosome 13: Associated with Patau syndrome, a condition characterized by severe intellectual disability and physical abnormalities
- Chromosome 18: Linked to Edwards syndrome, which involves multiple medical complications and developmental delays
- Chromosome 21: The chromosome responsible for Down syndrome, the most common chromosomal disorder
- Sex Chromosomes X and Y: Evaluates for conditions such as Turner syndrome (X0), Klinefelter syndrome (XXY), and other sex chromosome abnormalities
Who Should Consider This Genetic Screening?
This comprehensive chromosomal analysis is particularly recommended for:
- Pregnant women with abnormal ultrasound findings or screening results
- Couples with family histories of chromosomal disorders
- Women of advanced maternal age (35 years and older)
- Individuals with previous pregnancies affected by chromosomal abnormalities
- Cases where rapid chromosomal analysis is medically necessary
- Patients requiring prenatal diagnosis for informed pregnancy management
Significant Benefits of Chromosomal Analysis
Choosing our Chromosomes 13, 18, 21, X, Y Analysis provides numerous advantages:
- Rapid Results: Receive comprehensive findings within just 3-4 days
- High Accuracy: FISH technology delivers precise chromosomal evaluation
- Early Detection: Identify potential issues early for better preparation and management
- Comprehensive Screening: Covers the most common chromosomal abnormalities in a single test
- Informed Decision Making: Provides crucial information for medical and family planning decisions
- Minimal Sample Requirements: Uses small sample volumes for analysis
Understanding Your Test Results
Your Chromosomes 13, 18, 21, X, Y Analysis results will provide clear information about:
- Normal Results: Indicate typical chromosomal patterns with no detected abnormalities
- Aneuploidy Detection: Identifies extra or missing chromosomes (trisomy or monosomy)
- Sex Chromosome Status: Confirms typical (XX or XY) or atypical sex chromosome patterns
- Clinical Correlation: Results should always be discussed with your healthcare provider for proper interpretation
- Genetic Counseling: Abnormal results typically lead to referral for specialized genetic counseling
Test Pricing and Availability
| Test Component | Regular Price | Discount Price |
|---|---|---|
| Chromosomes 13, 18, 21, X, Y Analysis | $326 USD | $244 USD |
Nationwide Accessibility
GGC DNA maintains comprehensive testing facilities across major metropolitan areas throughout the United States. Our state-of-the-art laboratories serve patients in New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and numerous other cities. With convenient locations and streamlined sample collection processes, accessing advanced genetic testing has never been easier.
Take the Next Step in Genetic Health
Don’t leave your genetic health to chance. Our Chromosomes 13, 18, 21, X, Y Analysis provides the critical information you need for informed healthcare decisions. With rapid turnaround times, exceptional accuracy, and comprehensive coverage of the most significant chromosomal abnormalities, this test represents the gold standard in genetic screening.
Ready to schedule your test? Contact our genetic specialists today at +1(267) 388-9828 or book your appointment online. Our team is prepared to answer your questions and guide you through the testing process with compassion and expertise.
Note: This test requires a doctor’s prescription for most cases. Prescription requirements do not apply to surgery, pregnancy cases, or individuals planning international travel. Sample types accepted include amniotic fluid, chorionic villi, and cord blood collected in appropriate sterile containers.
