Chromosome Analysis Amniotic Fluid Test
Comprehensive Prenatal Chromosomal Screening
The Chromosome Analysis Amniotic Fluid Test represents a cornerstone of modern prenatal genetic diagnostics, offering expectant parents crucial insights into their baby’s chromosomal health. This sophisticated procedure examines fetal cells obtained through amniocentesis to detect chromosomal abnormalities that could impact fetal development and long-term health outcomes.
What This Test Measures and Detects
This advanced diagnostic test provides comprehensive analysis of fetal chromosomes through multiple detection methods:
- Chromosomal Number Abnormalities: Identifies conditions like Down syndrome (trisomy 21), Edwards syndrome (trisomy 18), and Patau syndrome (trisomy 13)
- Structural Chromosome Defects: Detects translocations, deletions, duplications, and inversions that may affect genetic material
- Sex Chromosome Abnormalities: Identifies conditions such as Turner syndrome, Klinefelter syndrome, and other sex chromosome variations
- Mosaic Patterns: Detects the presence of multiple cell lines with different chromosomal compositions
Who Should Consider This Test
This prenatal genetic screening is particularly recommended for:
- Women aged 35 years or older at delivery
- Abnormal first or second trimester screening results
- Previous pregnancy with chromosomal abnormalities
- Family history of genetic disorders or chromosomal conditions
- Abnormal ultrasound findings suggesting fetal anomalies
- Parents carrying balanced chromosomal rearrangements
- Unexplained recurrent pregnancy losses
Key Benefits of Chromosome Analysis
Choosing this comprehensive prenatal testing offers multiple advantages:
- Early Detection: Identifies chromosomal abnormalities during pregnancy, allowing for informed decision-making
- Comprehensive Analysis: Provides detailed information about all 46 chromosomes
- High Accuracy: Culture-based method ensures reliable results with minimal false positives
- Genetic Counseling Support: Results facilitate appropriate genetic counseling and management planning
- Peace of Mind: Normal results provide reassurance about fetal chromosomal health
Understanding Your Test Results
Your chromosome analysis report will provide detailed information about fetal chromosomal status:
- Normal Results: Indicate typical 46 chromosome count with normal male (46,XY) or female (46,XX) pattern
- Abnormal Results: Identify specific chromosomal abnormalities with detailed descriptions
- Mosaic Findings: Report the percentage of abnormal cells when mosaicism is detected
- Clinical Correlation: Results should be interpreted in context with ultrasound findings and clinical presentation
- Genetic Counseling: All abnormal results include recommendations for genetic counseling follow-up
Test Pricing Information
| Test Name | Discount Price | Regular Price |
|---|---|---|
| Chromosome Analysis Amniotic Fluid Test | $326 USD | $476 USD |
Nationwide Availability
We have diagnostic centers conveniently located across major cities in the United States, including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our specialized cytogenetics department ensures consistent, high-quality testing standards nationwide.
Book Your Test Today
Take the important step toward understanding your baby’s chromosomal health. Our experienced genetic counselors and specialized medical team are ready to support you through this process. Contact us today to schedule your Chromosome Analysis Amniotic Fluid Test and gain valuable insights into your pregnancy.
Call or WhatsApp: +1(267) 388-9828 to book your appointment or speak with our genetic counseling team.
