FLVCR2 Gene Hydranencephaly Fowler Type NGS Genetic DNA Test
Comprehensive Genetic Testing for Severe Brain Malformations
The FLVCR2 Gene Hydranencephaly Fowler Type NGS Genetic DNA Test represents a cutting-edge diagnostic approach for identifying genetic mutations associated with severe neurological conditions. This specialized test focuses on the FLVCR2 gene, which plays a critical role in normal brain development and function. Hydranencephaly Fowler type is an extremely rare congenital disorder characterized by the absence of cerebral hemispheres, replaced by cerebrospinal fluid-filled sacs.
What This Test Measures and Detects
Our advanced NGS Genetic DNA Test specifically targets:
- Mutations in the FLVCR2 gene responsible for Hydranencephaly Fowler type
- Single nucleotide variants (SNVs) and small insertions/deletions
- Copy number variations affecting the FLVCR2 gene region
- Pathogenic variants that disrupt normal brain development
- Inheritance patterns for genetic counseling purposes
Who Should Consider This Test
This genetic test is recommended for individuals presenting with:
- Prenatal ultrasound findings suggesting severe brain abnormalities
- Family history of Hydranencephaly or similar neurological conditions
- Infants with unexplained neurological symptoms and developmental delays
- Parents planning pregnancy with known family history of FLVCR2 mutations
- Individuals with suspected genetic predisposition to brain malformations
Key Symptoms and Clinical Indications
Clinical features that may indicate the need for FLVCR2 gene testing include:
- Severe microcephaly or abnormal head size at birth
- Neurological abnormalities detected during prenatal screening
- Developmental delays and failure to thrive
- Seizures and other neurological manifestations
- Family history of similar congenital brain disorders
Benefits of FLVCR2 Genetic Testing
Comprehensive Diagnostic Advantages
Undergoing the FLVCR2 Gene Hydranencephaly Fowler Type NGS Genetic DNA Test provides numerous benefits:
- Definitive Diagnosis: Provides conclusive genetic evidence for suspected conditions
- Family Planning Guidance: Enables informed reproductive decisions for at-risk families
- Early Intervention: Facilitates timely medical management and supportive care
- Genetic Counseling: Supports comprehensive family genetic risk assessment
- Research Contribution: Helps advance understanding of rare genetic disorders
Advanced Technology Benefits
Our NGS-based approach offers superior advantages:
- High accuracy and sensitivity in mutation detection
- Comprehensive analysis of the entire FLVCR2 gene
- Ability to detect various types of genetic variations
- Rapid turnaround time of 3-4 weeks
- Minimal sample requirements with multiple collection options
Understanding Your Test Results
Interpreting Genetic Findings
Your FLVCR2 gene test results will be carefully interpreted by our genetic specialists:
Positive Result
A positive result indicates the presence of pathogenic mutations in the FLVCR2 gene, confirming the diagnosis of Hydranencephaly Fowler type. This information is crucial for:
- Confirming clinical diagnosis
- Guiding medical management strategies
- Providing accurate genetic counseling
- Assessing recurrence risks for future pregnancies
Negative Result
A negative result suggests that no pathogenic FLVCR2 mutations were detected. However, this doesn’t completely rule out the condition, as:
- Rare mutations might not be detected by current technology
- Other genetic or environmental factors could be involved
- Further testing may be recommended based on clinical presentation
Variant of Uncertain Significance (VUS)
Some results may identify genetic changes with unknown clinical significance. In such cases:
- Additional family studies may be recommended
- Ongoing research may provide future clarity
- Clinical correlation remains essential
Test Pricing and Availability
| Test Component | Price (USD) | Details |
|---|---|---|
| Discount Price | $500 | Limited time offer including genetic counseling |
| Regular Price | $700 | Standard pricing for comprehensive testing |
Test Specifications
- Turnaround Time: 3-4 Weeks
- Sample Type: Blood, Extracted DNA, or One Drop Blood on FTA Card
- Methodology: Next-Generation Sequencing (NGS) Technology
- Specialty: Pediatric Genetics
- Department: Genetics
Pre-Test Requirements
Essential Preparation Steps
Before undergoing the FLVCR2 Gene Hydranencephaly Fowler Type NGS Genetic DNA Test, patients should:
- Provide complete clinical history relevant to FLVCR2 Gene Hydranencephaly
- Participate in a Genetic Counseling session
- Provide detailed family medical history
- Complete pedigree chart documentation of affected family members
- Understand the implications and limitations of genetic testing
Nationwide Availability
We proudly serve patients across the United States with convenient testing locations in all major cities including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many more. Our network of certified genetic counselors and medical professionals ensures accessible, high-quality care regardless of your location.
Take the Next Step Toward Genetic Clarity
Don’t let uncertainty about genetic conditions affect your family’s future. The FLVCR2 Gene Hydranencephaly Fowler Type NGS Genetic DNA Test provides the answers you need for informed medical decisions and family planning.
Ready to schedule your test? Contact our genetic specialists today:
Phone: +1(267) 388-9828
WhatsApp: +1(267) 388-9828
Our dedicated team is available to answer your questions, discuss testing options, and help you understand the process. Take control of your genetic health with comprehensive, accurate testing from General Genetics Corporation.
