Prenatal Diagnosis Panel 2 Amniotic Fluid Test
Comprehensive Genetic Screening for Your Peace of Mind
The Prenatal Diagnosis Panel 2 Amniotic Fluid Test represents a cutting-edge approach to prenatal genetic diagnosis, specifically designed to detect inborn errors of metabolism that could significantly impact fetal development and long-term health outcomes. This specialized screening utilizes advanced two-dimensional electrophoresis technology to analyze amniotic fluid samples, providing expectant parents with crucial information about potential genetic conditions during the critical second trimester of pregnancy.
What This Test Measures and Detects
Our Prenatal Diagnosis Panel 2 focuses primarily on identifying mucopolysaccharidoses (MPS), a group of metabolic disorders caused by the absence or malfunctioning of specific lysosomal enzymes needed to break down complex carbohydrates called glycosaminoglycans. The test specifically measures:
- Enzyme activity levels for various mucopolysaccharidosis types
- Biochemical markers indicating metabolic dysfunction
- Genetic indicators of inherited metabolic conditions
- Specific protein patterns associated with storage disorders
Who Should Consider This Prenatal Screening
This advanced genetic screening is particularly recommended for:
- Couples with family history of metabolic disorders
- Parents who have previously had a child with mucopolysaccharidoses
- Women with abnormal ultrasound findings suggesting skeletal or organ abnormalities
- Cases where carrier screening has identified potential genetic risks
- Pregnancies where advanced maternal age or other risk factors are present
Clinical Indications and Symptoms Warranting Testing
While this is primarily a screening test, certain clinical scenarios strongly indicate the need for comprehensive prenatal diagnosis:
- Family history of lysosomal storage diseases
- Previous pregnancy affected by metabolic disorders
- Abnormal biochemical screening results
- Consanguineous relationships increasing genetic risk
- Ethnic backgrounds with higher prevalence of specific metabolic conditions
Significant Benefits of Early Detection
Choosing the Prenatal Diagnosis Panel 2 Amniotic Fluid Test offers numerous advantages for expectant families:
- Early Intervention Planning: Allows for preparation and specialized care if needed
- Informed Decision Making: Provides crucial information for medical and family planning
- Reduced Anxiety: Offers peace of mind through comprehensive screening
- Specialized Care Coordination: Enables early connection with pediatric genetic specialists
- Treatment Preparation: Facilitates arrangements for potential enzyme replacement therapies
- Family Education: Helps families understand and prepare for specific health needs
Understanding Your Test Results
Our comprehensive reporting system provides clear, understandable results:
- Normal Results: Indicate typical enzyme activity levels and no detected metabolic abnormalities
- Abnormal Results: Suggest potential metabolic disorders requiring further evaluation
- Borderline Findings: May indicate carrier status or mild enzyme deficiencies
- Comprehensive Interpretation: Each report includes detailed explanations and recommended next steps
Post-Test Guidance and Support
Regardless of your results, our genetic counseling team provides:
- Detailed result interpretation sessions
- Connections to appropriate medical specialists
- Resources for further testing if indicated
- Support for decision-making processes
- Referrals to patient support organizations
Test Pricing and Availability
| Price Type | Amount (USD) |
|---|---|
| Discount Price | $146 |
| Regular Price | $162 |
Testing Process and Timeline
Our streamlined testing process ensures accuracy and timely results:
- Sample Collection: Amniotic fluid collected after 16 weeks gestation
- Sample Requirements: 10 mL minimum volume in sterile container
- Transport: Maintained at 18-22°C and shipped within 24 hours
- Turnaround Time: Results available within 10 days
- Daily Processing: Samples accepted until 4 PM daily
Nationwide Accessibility
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, and many other cities. Our network of certified collection centers ensures accessible prenatal genetic testing services nationwide.
Take the Next Step Toward Comprehensive Prenatal Care
Don’t leave your prenatal health to chance. Our Prenatal Diagnosis Panel 2 Amniotic Fluid Test provides the advanced screening capabilities you need for complete peace of mind during your pregnancy journey. With specialized genetic expertise and state-of-the-art laboratory technology, we’re committed to delivering accurate, timely results that empower your healthcare decisions.
Ready to schedule your prenatal genetic screening? Contact our genetic counseling team today at +1(267) 388-9828 or book your appointment online. Our compassionate professionals are available to answer your questions and guide you through the testing process with the care and expertise your family deserves.
