Molecular Karyotyping for Amniotic Fluid Test
Comprehensive Prenatal Genetic Analysis
Molecular Karyotyping for Amniotic Fluid Test represents a cutting-edge advancement in prenatal genetic diagnostics. This sophisticated procedure provides expectant parents with detailed chromosomal analysis of the developing fetus, offering invaluable insights into genetic health and development. By examining amniotic fluid samples through advanced cell culture techniques, our specialized laboratory delivers comprehensive chromosomal assessment with exceptional accuracy and reliability.
What Does This Test Measure and Detect?
Our Molecular Karyotyping test provides comprehensive detection of chromosomal abnormalities through detailed analysis of fetal cells:
- Numerical chromosomal abnormalities including trisomies (Down syndrome, Edwards syndrome, Patau syndrome)
- Structural chromosomal variations such as deletions, duplications, and translocations
- Sex chromosome abnormalities including Turner syndrome and Klinefelter syndrome
- Microdeletions and microduplications that may impact fetal development
- Mosaicism and chromosomal rearrangements
Who Should Consider Molecular Karyotyping?
This advanced prenatal testing 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 loss
Key Benefits of Molecular Karyotyping
Choosing our Molecular Karyotyping test provides numerous advantages for expectant parents:
- Comprehensive Detection: Identifies both numerical and structural chromosomal abnormalities
- High Accuracy: Advanced cell culture techniques ensure reliable results
- Early Intervention: Enables informed decision-making and appropriate medical management
- Peace of Mind: Provides reassurance about fetal chromosomal health
- Expert Interpretation: Results analyzed by board-certified genetic specialists
- Rapid Turnaround: Results typically available within 7-9 days
Understanding Your Test Results
Our comprehensive reporting system ensures you receive clear, understandable results:
- Normal Results: Indicate typical chromosomal patterns with no detected abnormalities
- Abnormal Results: Detailed explanation of specific chromosomal findings
- Genetic Counseling: Access to certified genetic counselors for result interpretation
- Clinical Correlation: Results correlated with ultrasound findings and clinical presentation
- Follow-up Recommendations: Guidance on next steps and additional testing if needed
Test Pricing Information
| Price Type | Amount (USD) |
|---|---|
| Discount Price | $450 |
| Regular Price | $512 |
Nationwide Testing Availability
We proudly serve patients across the United States with convenient testing locations in all major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many more. Our network of certified laboratories and collection centers ensures accessible prenatal genetic testing nationwide.
Schedule Your Test Today
Take the next step in ensuring your baby’s genetic health. Our experienced team is ready to assist you with scheduling, questions, and support throughout the testing process. Contact us today to book your Molecular Karyotyping for Amniotic Fluid Test and gain the peace of mind you deserve.
Call or WhatsApp: +1(267) 388-9828
Our genetic specialists are available to discuss your testing needs, answer questions, and help you schedule your appointment at a convenient location near you.
