Comprehensive Prenatal Diagnosis Panel 1 Chorionic Villus Biopsy Test available for $1170 USD across USA. Early detection of 8 metabolic disorders including GM1 Gangliosidosis
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Prenatal Diagnosis Panel 1 Chorionic Villus Biopsy Test

Original price was: $1,300.Current price is: $1,170.

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The Prenatal Diagnosis Panel 1 Chorionic Villus Biopsy Test is a comprehensive genetic screening procedure performed between 10-13 weeks of pregnancy. This advanced diagnostic test detects eight critical inborn errors of metabolism through enzyme assay analysis of chorionic villus samples. The panel screens for life-threatening conditions including Metachromatic Leucodystrophy, GM1 Gangliosidosis, GM2 Gangliosidosis, Gaucher Disease, Niemann Pick Disease, Fabry Disease, Pompe Disease, and MPS-1 (Hurler Syndrome). This early detection allows for informed family planning decisions and specialized medical management. The test is priced at $1170 USD with a regular price of $1300 USD, providing significant savings for comprehensive prenatal genetic screening.

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Prenatal Diagnosis Panel 1 Chorionic Villus Biopsy Test

Comprehensive Early Genetic Screening for Metabolic Disorders

The Prenatal Diagnosis Panel 1 Chorionic Villus Biopsy Test represents a breakthrough in prenatal genetic diagnostics, offering expectant parents crucial information about their baby’s health during the first trimester. This sophisticated screening procedure is performed between 10-13 weeks gestation and provides early detection of eight severe metabolic disorders that can significantly impact a child’s development and quality of life.

What This Advanced Test Detects

Our comprehensive panel utilizes cutting-edge enzyme assay technology to screen for the following critical inborn errors of metabolism:

  • Metachromatic Leucodystrophy (Code Y556) – A progressive nervous system disorder affecting myelin formation
  • GM1 Gangliosidosis (Code Y557) – A lysosomal storage disease causing progressive neurological deterioration
  • GM2 Gangliosidosis (Code Y558) – Includes Tay-Sachs disease and related conditions
  • Gaucher Disease (Code Y559) – A disorder affecting multiple organ systems including liver, spleen, and bones
  • Niemann Pick Disease (Code Y560) – A group of inherited metabolic disorders affecting lipid storage
  • Fabry Disease (Code Y561) – A condition causing progressive damage to kidneys, heart, and nervous system
  • Pompe Disease (Code Y562) – A glycogen storage disease affecting muscle function
  • MPS-1 (Hurler Syndrome) (Code Y563) – A severe mucopolysaccharidosis affecting multiple body systems

Who Should Consider This Essential Screening?

This prenatal diagnostic test is particularly recommended for:

  • Couples with family history of metabolic disorders
  • Parents who have previously had a child affected by any of these conditions
  • Individuals from ethnic backgrounds with higher prevalence of specific metabolic diseases
  • Couples seeking comprehensive early genetic information
  • Those with abnormal ultrasound findings suggesting metabolic disorders

Critical Benefits of Early Detection

Choosing the Prenatal Diagnosis Panel 1 offers numerous advantages:

  • Early Intervention Planning – Allows families and healthcare providers to prepare for specialized care needs
  • Informed Decision Making – Provides crucial information for family planning and medical management
  • Peace of Mind – Offers reassurance when results are normal or prepares families for potential challenges
  • Comprehensive Screening – Tests for eight different conditions in a single procedure
  • Early Timeline – Performed during first trimester for timely information

Understanding Your Test Results

Our genetic counseling team provides comprehensive interpretation of your results:

  • Normal Results – Indicate no detected abnormalities in the screened metabolic pathways
  • Abnormal Results – Suggest potential metabolic disorders requiring further evaluation
  • Inconclusive Results – May require additional testing or follow-up procedures

All results are reviewed by board-certified genetic specialists who provide detailed explanations and guidance for next steps. Our team ensures you understand the implications of your results and available options.

Test Pricing and Availability

Price Type Amount (USD)
Discount Price $1170
Regular Price $1300

Nationwide Accessibility

We have conveniently located branches across the United States, serving major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many other cities. Our network ensures accessible genetic testing services for families nationwide.

Schedule Your Prenatal Genetic Screening Today

Take the proactive step toward comprehensive prenatal care. Our experienced genetic counselors and medical professionals are ready to guide you through this important screening process. Contact us today to schedule your appointment and discuss your testing options.

Call or WhatsApp: +1(267) 388-9828

Our team is available to answer your questions, explain the procedure in detail, and help you make informed decisions about your prenatal care. Early detection through the Prenatal Diagnosis Panel 1 Chorionic Villus Biopsy Test provides valuable information for your family’s health journey.

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