Chromosome Analysis High Resolution Neonatal Test
Comprehensive Genetic Screening for Newborn Health
The Chromosome Analysis High Resolution Neonatal Test represents a cutting-edge diagnostic approach specifically designed for infants and newborns. This sophisticated genetic screening utilizes advanced high-resolution karyotyping technology to provide unparalleled insight into your baby’s chromosomal health. By examining the complete chromosomal structure with exceptional detail, this test can identify subtle abnormalities that standard chromosomal analyses might miss, offering parents and healthcare providers critical information for early intervention and personalized care planning.
What Does This Test Measure and Detect?
Our High Resolution Neonatal Test conducts a comprehensive examination of your newborn’s chromosomes, focusing on several key areas:
- Chromosomal Number Abnormalities: Detects conditions like Down syndrome (trisomy 21), Edwards syndrome (trisomy 18), and Patau syndrome (trisomy 13)
- Structural Chromosomal Variations: Identifies deletions, duplications, translocations, and inversions that may impact development
- Microdeletion Syndromes: Detects small chromosomal deletions associated with specific genetic conditions
- Sex Chromosome Abnormalities: Identifies variations in X and Y chromosomes that may affect development
- Marker Chromosomes: Detects small extra chromosomes of unknown origin
Who Should Consider This Test?
This specialized neonatal chromosomal analysis is recommended for infants presenting with:
- Multiple congenital anomalies or unusual physical features
- Developmental delays or failure to thrive
- Family history of chromosomal disorders or genetic conditions
- Abnormal prenatal screening results
- Unexplained growth restrictions or feeding difficulties
- Suspected genetic syndromes based on clinical presentation
- History of multiple miscarriages or stillbirths in the family
Key Benefits of High Resolution Neonatal Chromosome Analysis
Choosing our comprehensive chromosomal screening offers numerous advantages for your newborn’s health journey:
- Early Intervention Opportunities: Enables timely medical interventions and therapeutic approaches
- Accurate Diagnosis: Provides definitive answers about suspected genetic conditions
- Family Planning Guidance: Offers valuable information for future family planning decisions
- Personalized Care Planning: Helps healthcare providers develop targeted treatment strategies
- Peace of Mind: Provides clarity and reduces uncertainty about your baby’s genetic health
- Comprehensive Assessment: High-resolution technology detects subtle abnormalities missed by standard tests
Understanding Your Test Results
Our comprehensive report provides detailed information about your newborn’s chromosomal analysis:
- Normal Results: Indicate typical chromosomal structure and number, providing reassurance about genetic health
- Abnormal Findings: Detailed explanation of any chromosomal variations detected, including potential implications
- Clinical Correlation: Guidance on how findings relate to your baby’s specific health concerns
- Follow-up Recommendations: Suggestions for additional testing or specialist consultations if needed
- Genetic Counseling: Information about the inheritance patterns and recurrence risks
Test Pricing and Details
| Test Name | Regular Price | Discount Price |
|---|---|---|
| Chromosome Analysis High Resolution Neonatal Test | $120 USD | $108 USD |
Test Specifications
- Turnaround Time: Sample accepted daily by 6 pm; Report delivered in 21 working days
- Sample Type: 4 ml (2 ml minimum) whole blood in 1 Green top (Sodium Heparin) tube
- Shipping Instructions: Ship refrigerated immediately. DO NOT FREEZE
- Required Documentation: Duly filled Chromosome & FISH Analysis Requisition form (Form 17) is mandatory
- Methodology: Culture, Microscopy, High Resolution Karyotype
Nationwide Accessibility Across the United States
We proudly serve families 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, Austin, Jacksonville, Fort Worth, Columbus, Charlotte, San Francisco, Indianapolis, Seattle, Denver, Washington DC, Boston, El Paso, Nashville, Detroit, Oklahoma City, Portland, Las Vegas, Memphis, Louisville, Baltimore, and Milwaukee. Our extensive network ensures that comprehensive genetic testing is accessible to families nationwide.
Take the Next Step for Your Newborn’s Health
Don’t leave questions about your baby’s genetic health unanswered. Our Chromosome Analysis High Resolution Neonatal Test provides the clarity and information you need to make informed decisions about your newborn’s care. With our discounted price of only $108 USD and comprehensive nationwide coverage, there’s no reason to delay this important genetic assessment.
Book your appointment today by calling our dedicated genetics specialists at +1(267) 388-9828 or schedule online through our secure booking portal. Our team is ready to answer your questions and guide you through the testing process with compassion and expertise.
