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Peripheral Blood Karyotyping for Couples

Original price was: $226.Current price is: $190.

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Peripheral Blood Karyotyping for Couples is a comprehensive genetic screening test that analyzes chromosomal structure and number in both partners. This advanced diagnostic procedure helps identify potential genetic abnormalities that could impact fertility, pregnancy outcomes, and future offspring health. The test examines 46 chromosomes for structural abnormalities, numerical disorders, and balanced translocations that may not show symptoms in carriers but can cause serious conditions in children. At just $190 USD, this test provides invaluable insights for couples planning pregnancy, experiencing recurrent miscarriages, or with family histories of genetic disorders. Results are typically available within 10-12 days, providing couples with essential genetic information to make informed family planning decisions.

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  • ISO-Accredited Laboratory, Ensuring Highest Standards
  • Trusted by Hospitals & Patients —Accredited Testing with Results
  • Direct Healthcare Provider Support + Comprehensive Reporting
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Peripheral Blood Karyotyping for Couples: Comprehensive Chromosomal Analysis

Understanding Couple Karyotyping: A Vital Genetic Screening Tool

Peripheral Blood Karyotyping for Couples represents a cornerstone of modern genetic medicine, providing comprehensive chromosomal analysis for individuals planning to start a family. This sophisticated diagnostic procedure examines the complete chromosomal makeup of both partners, offering critical insights into potential genetic factors that could influence fertility, pregnancy outcomes, and the health of future children. By analyzing chromosomal structure and number, this test helps identify hidden genetic conditions that may not manifest symptoms in carriers but can have significant implications for offspring.

What Does Couple Karyotyping Measure and Detect?

This advanced genetic screening test provides detailed analysis of several key chromosomal components:

  • Chromosomal Number Abnormalities: Detects conditions like Down syndrome (trisomy 21), Edwards syndrome (trisomy 18), and Turner syndrome (monosomy X)
  • Structural Chromosomal Defects: Identifies translocations, deletions, duplications, and inversions that may affect genetic material
  • Balanced Translocations: Reveals rearrangements where genetic material is exchanged between chromosomes without loss or gain
  • Mosaicism: Detects the presence of two or more cell lines with different chromosomal compositions
  • Marker Chromosomes: Identifies small, abnormal chromosomes that may contain critical genetic material

Who Should Consider Couple Karyotyping?

This comprehensive genetic screening is particularly recommended for couples in the following situations:

Primary Indications for Testing

  • Couples Planning Pregnancy: Proactive screening before conception to identify potential genetic risks
  • Recurrent Pregnancy Loss: Two or more consecutive miscarriages warrant chromosomal investigation
  • Family History of Genetic Disorders: Known chromosomal conditions in family members
  • Advanced Maternal Age: Women over 35 planning pregnancy
  • Unexplained Infertility: Couples experiencing difficulty conceiving without clear cause
  • Previous Child with Chromosomal Abnormalities: Families with affected children seeking genetic counseling
  • Consanguineous Marriages: Couples who are blood relatives

Significant Benefits of Couple Karyotyping

Undergoing peripheral blood karyotyping offers numerous advantages for couples planning their reproductive future:

Comprehensive Genetic Insights

  • Informed Family Planning: Make educated decisions about pregnancy timing and preparation
  • Risk Assessment: Understand the probability of passing genetic conditions to offspring
  • Early Intervention Planning: Prepare for potential special needs and medical requirements
  • Peace of Mind: Reduce anxiety about unknown genetic factors affecting pregnancy
  • Reproductive Options: Explore alternative family building methods if indicated

Understanding Your Karyotyping Results

Interpreting karyotyping results requires professional genetic counseling, but here’s a general guide to understanding your report:

Normal Results Interpretation

  • 46,XX (Female): Normal female chromosomal pattern
  • 46,XY (Male): Normal male chromosomal pattern
  • No Structural Abnormalities: Chromosomes appear normal in size, shape, and banding pattern

Abnormal Findings and Their Implications

  • Balanced Translocations: No genetic material lost, but increased risk for unbalanced offspring
  • Numerical Abnormalities: Extra or missing chromosomes affecting fertility or pregnancy
  • Structural Rearrangements: May impact gene function and reproductive outcomes

Test Details and Pricing

Test Component Details
Test Name Peripheral Blood Karyotyping for Couples
Regular Price $226 USD
Discount Price $190 USD
Turnaround Time 10-12 days
Sample Type Peripheral Blood
Test Components Sodium Heparin Vacutainer (2ml)
Method Cell Culture

Pre-Test Instructions and Requirements

Peripheral Blood Karyotyping for Couples requires a Doctor’s prescription for most cases. However, prescription requirements do not apply for:

  • Surgery preparation cases
  • >Pregnancy-related testing

  • Individuals planning international travel requiring genetic screening

Nationwide Accessibility

We proudly serve couples 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 state-of-the-art laboratories ensure consistent, reliable results regardless of location.

Take the Next Step in Your Genetic Health Journey

Don’t leave your family’s genetic health to chance. Our comprehensive Peripheral Blood Karyotyping for Couples provides the critical information needed for informed reproductive decisions. With rapid 10-12 day turnaround and affordable pricing at just $190 USD, there’s never been a better time to invest in your genetic future.

Ready to begin your genetic screening journey? Contact our genetic specialists today at +1(267) 388-9828 to schedule your appointment or discuss your testing options. Our compassionate team is here to guide you through every step of the process, ensuring you receive the comprehensive care and support you deserve.