TFAP2B Gene Char Syndrome NGS Genetic DNA Test
Comprehensive Genetic Analysis for Char Syndrome Detection
The TFAP2B Gene Char Syndrome NGS Genetic DNA Test represents a cutting-edge diagnostic approach for identifying mutations in the TFAP2B gene, which are responsible for Char Syndrome – a rare congenital disorder affecting multiple body systems. This sophisticated genetic testing utilizes Next-Generation Sequencing technology to provide comprehensive analysis of the TFAP2B gene, enabling precise detection of pathogenic variants that contribute to this complex condition.
What Does the TFAP2B Gene Char Syndrome Test Measure?
This advanced genetic test specifically targets and analyzes the TFAP2B (Transcription Factor AP-2 Beta) gene, which plays a crucial role in embryonic development and tissue differentiation. The test detects:
- Point mutations and small insertions/deletions in the TFAP2B gene
- Pathogenic variants associated with Char Syndrome development
- Genetic alterations affecting protein function and gene regulation
- Inheritance patterns for family genetic counseling purposes
Who Should Consider This Genetic Test?
This specialized genetic testing is recommended for individuals presenting with:
- Characteristic facial dysmorphisms including broad nasal bridge and down-slanting palpebral fissures
- Hand abnormalities such as fifth finger clinodactyly or syndactyly
- Congenital heart defects, particularly patent ductus arteriosus
- Developmental delays or intellectual disabilities
- Family history of Char Syndrome or similar congenital conditions
- Unexplained multiple congenital anomalies
Significant Benefits of TFAP2B Genetic Testing
Undergoing this comprehensive genetic analysis provides numerous advantages:
- Accurate Diagnosis: Precise identification of TFAP2B gene mutations confirms Char Syndrome diagnosis
- Personalized Treatment Planning: Enables targeted medical interventions based on genetic findings
- Family Planning Guidance: Provides crucial information for reproductive decision-making
- Early Intervention Opportunities: Facilitates timely medical management and therapeutic approaches
- Genetic Counseling Support: Comprehensive pre-test and post-test genetic counseling included
Understanding Your Test Results
Our expert genetic counselors will provide detailed interpretation of your TFAP2B Gene Char Syndrome NGS Genetic DNA Test results:
- Positive Result: Indicates the presence of pathogenic TFAP2B gene mutation, confirming Char Syndrome diagnosis
- Negative Result: Suggests absence of detectable TFAP2B mutations, though clinical correlation remains essential
- Variant of Uncertain Significance: Identifies genetic changes requiring further clinical evaluation
- Carrier Status: Determines inheritance patterns and recurrence risks for family members
Test Details and Pricing
| Test Component | Details |
|---|---|
| Test Name | TFAP2B Gene Char Syndrome NGS Genetic DNA Test |
| Regular Price | $700 USD |
| Discount Price | $500 USD |
| Turnaround Time | 3 to 4 Weeks |
| Sample Type | Blood, Extracted DNA, or One Drop Blood on FTA Card |
| Testing Method | Next-Generation Sequencing (NGS) Technology |
Pre-Test Requirements
Before undergoing the TFAP2B Gene Char Syndrome NGS Genetic DNA Test, patients should provide:
- Complete clinical history detailing symptoms and developmental concerns
- Participation in genetic counseling session to create comprehensive family pedigree
- Documentation of any previous genetic testing or medical evaluations
- Information about affected family members and their medical conditions
Nationwide Testing Availability
We proudly offer the TFAP2B Gene Char Syndrome NGS Genetic DNA Test across our extensive network of testing facilities throughout the United States. Our state-of-the-art laboratories and experienced genetic specialists ensure consistent, high-quality testing services in major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose.
Take Control of Your Genetic Health Today
Don’t wait to get the answers you need about Char Syndrome and TFAP2B gene mutations. Our comprehensive genetic testing provides the clarity required for informed medical decisions and personalized care planning. With our discounted price of only $500 USD and nationwide availability, accessing advanced genetic testing has never been more convenient.
Call or WhatsApp us now at +1(267) 388-9828 to schedule your TFAP2B Gene Char Syndrome NGS Genetic DNA Test and begin your journey toward genetic clarity and personalized medical management.
