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Prenatal Diagnostic Screening by Karyotyping

Original price was: $400.Current price is: $300.

-25%

Prenatal Diagnostic Screening by Karyotyping is a comprehensive genetic test that analyzes fetal chromosomes to detect abnormalities during pregnancy. This advanced diagnostic procedure examines the complete chromosomal structure through cell culture techniques, identifying conditions like Down syndrome, Edwards syndrome, and Patau syndrome. The test provides crucial information about fetal development and helps expectant parents make informed decisions. With a turnaround time of 15-20 days, this screening offers reliable results using amniotic fluid or chorionic tissue samples. Available for $300 USD, this essential prenatal testing is recommended for high-risk pregnancies, advanced maternal age, or abnormal ultrasound findings. Our nationwide network ensures accessible testing across major US cities.

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Prenatal Diagnostic Screening by Karyotyping

Comprehensive Chromosomal Analysis for Pregnancy Health

Prenatal Diagnostic Screening by Karyotyping represents a cornerstone of modern obstetric care, providing expectant parents with critical insights into their baby’s genetic health. This sophisticated diagnostic procedure examines the complete chromosomal makeup of developing fetuses, offering unparalleled accuracy in detecting chromosomal abnormalities that could impact fetal development and long-term health outcomes.

What Does Karyotyping Measure and Detect?

This advanced genetic screening employs cell culture techniques to analyze fetal chromosomes in meticulous detail. The test specifically identifies:

  • Numerical Chromosomal Abnormalities: Detects conditions like Down syndrome (Trisomy 21), Edwards syndrome (Trisomy 18), and Patau syndrome (Trisomy 13)
  • Structural Chromosomal Variations: Identifies translocations, deletions, duplications, and inversions that may affect genetic function
  • Sex Chromosome Abnormalities: Screens for conditions such as Turner syndrome, Klinefelter syndrome, and other sex chromosome variations
  • Mosaic Patterns: Detects mixed cell populations with different chromosomal compositions

Who Should Consider Prenatal Karyotyping?

This essential screening is particularly recommended for:

  • Women aged 35 years or older at delivery
  • Couples with family history of chromosomal disorders
  • Previous pregnancy with chromosomal abnormalities
  • Abnormal ultrasound findings suggesting fetal anomalies
  • Positive results from initial screening tests
  • Parents carrying balanced chromosomal rearrangements
  • Unexplained recurrent pregnancy loss

Significant Benefits of Prenatal Chromosomal Analysis

Choosing prenatal karyotyping provides numerous advantages for expectant families:

  • Early Detection: Identifies potential issues weeks before birth, allowing for proper medical planning
  • Comprehensive Assessment: Examines all 46 chromosomes for complete genetic evaluation
  • Accurate Diagnosis: Provides definitive results with high specificity and sensitivity
  • Informed Decision-Making: Empowers parents with crucial information for pregnancy management
  • Psychological Preparation: Helps families prepare for potential special needs
  • Medical Team Coordination: Enables early involvement of pediatric specialists when needed

Understanding Your Test Results

Your karyotyping results will provide detailed information about your baby’s chromosomal health:

  • Normal Results: Indicate typical chromosomal patterns with 46 chromosomes arranged in 23 pairs
  • Abnormal Findings: Will specify the exact chromosomal variation detected and its potential implications
  • Genetic Counseling: All abnormal results include consultation with certified genetic counselors
  • Clinical Correlation: Results are interpreted in context with ultrasound findings and clinical presentation
  • Follow-up Recommendations: Includes guidance for additional testing or monitoring when indicated

Test Pricing and Details

Test Component Details
Test Name Prenatal Diagnostic Screening by Karyotyping
Discount Price $300 USD
Regular Price $400 USD
Turnaround Time 15-20 days
Sample Type Amniotic fluid / Bits of Chorionic tissue
Test Components 2 sterile tubes (15 ml each) / Sterile tissue culture container
Specialty Gynecologist
Method Cell Culture

Nationwide Accessibility

We maintain comprehensive testing facilities across the United States, with specialized centers in major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, and numerous other cities. Our network ensures that expectant parents nationwide have access to this critical prenatal screening with consistent quality standards and reliable turnaround times.

Book Your Prenatal Screening Today

Take the important step toward comprehensive prenatal care. Our experienced genetic specialists and state-of-the-art laboratory facilities ensure the highest standards of accuracy and reliability. Contact us today to schedule your Prenatal Diagnostic Screening by Karyotyping and gain valuable insights into your baby’s genetic health.

Call or WhatsApp: +1(267) 388-9828 to book your appointment or discuss your testing needs with our genetic counseling team.

Note: Prenatal Diagnostic Screening by Karyotyping requires a doctor’s prescription. Prescription requirements do not apply for surgery and pregnancy cases or individuals planning international travel.