CD36 Gene Platelet Glycoprotein IV Deficiency NGS Genetic DNA Test
Comprehensive Introduction to CD36 Genetic Testing
The CD36 Gene Platelet Glycoprotein IV Deficiency NGS Genetic DNA Test represents a cutting-edge diagnostic approach for identifying inherited platelet disorders. This specialized genetic analysis focuses on the CD36 gene, which encodes platelet glycoprotein IV—a crucial membrane protein essential for proper platelet function and coagulation processes. Understanding your genetic predisposition to platelet abnormalities can significantly impact your hematological health management and treatment strategies.
Platelet glycoprotein IV deficiency, also known as CD36 deficiency, is an inherited condition that affects platelet aggregation and can lead to various bleeding manifestations. Our advanced Next-Generation Sequencing (NGS) technology provides unparalleled accuracy in detecting mutations within the CD36 gene, offering patients and healthcare providers definitive diagnostic information for informed medical decision-making.
What This Test Measures and Detects
The CD36 Gene Platelet Glycoprotein IV Deficiency NGS Genetic DNA Test specifically analyzes:
- Complete sequencing of the CD36 gene to identify pathogenic variants
- Mutations affecting platelet glycoprotein IV expression and function
- Genetic markers associated with inherited platelet disorders
- Variants that may impact platelet aggregation and coagulation
- Both known and novel mutations using comprehensive NGS technology
This test provides a comprehensive genetic profile that helps determine whether an individual carries mutations that could lead to platelet glycoprotein IV deficiency, enabling early intervention and appropriate management strategies.
Who Should Consider CD36 Genetic Testing
This specialized genetic test is particularly recommended for individuals experiencing:
- Unexplained bruising or prolonged bleeding after minor injuries
- Abnormal platelet counts or function test results
- Family history of bleeding disorders or platelet abnormalities
- Recurrent nosebleeds or gum bleeding without apparent cause
- Heavy menstrual bleeding in women
- Previous abnormal bleeding during surgical procedures
- Diagnostic uncertainty regarding hematological symptoms
Additionally, individuals with a confirmed family history of CD36 deficiency or those planning pregnancy with concerns about inherited bleeding disorders should consider this comprehensive genetic analysis.
Significant Benefits of CD36 Genetic Testing
Undergoing the CD36 Gene Platelet Glycoprotein IV Deficiency NGS Genetic DNA Test provides numerous advantages:
- Accurate Diagnosis: Provides definitive identification of CD36 gene mutations
- Personalized Treatment: Enables tailored management strategies based on genetic findings
- Family Planning Guidance: Offers valuable information for reproductive decisions
- Early Intervention: Facilitates proactive management of potential bleeding risks
- Comprehensive Analysis: Utilizes advanced NGS technology for thorough genetic assessment
- Expert Interpretation: Includes professional genetic counseling and result explanation
Understanding Your Test Results
Your CD36 genetic test results will be carefully interpreted by our expert genetic counselors and hematologists. A positive result indicating CD36 gene mutations suggests an increased risk for platelet glycoprotein IV deficiency and associated bleeding tendencies. Negative results typically indicate that no pathogenic variants were detected in the CD36 gene, though clinical correlation with symptoms remains important.
Our comprehensive post-test counseling ensures you fully understand your results and their implications for your health management. We provide detailed guidance on:
- Interpreting genetic variants and their clinical significance
- Management strategies for identified mutations
- Family member testing recommendations
- Lifestyle considerations and precautions
- Follow-up testing and monitoring requirements
Test Pricing and Details
| Test Component | Details |
|---|---|
| Test Name | CD36 Gene Platelet Glycoprotein IV Deficiency NGS Genetic DNA Test |
| Discount Price | $500 USD |
| Regular Price | $700 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 |
Nationwide Testing Availability
We proudly offer the CD36 Gene Platelet Glycoprotein IV Deficiency NGS Genetic DNA Test across our extensive network of testing facilities throughout the United States. Our state-of-the-art laboratories and collection centers are conveniently located in major metropolitan areas including:
- New York City and surrounding regions
- Los Angeles and Southern California
- Chicago and the Midwest
- Houston and Texas metropolitan areas
- Phoenix and Arizona locations
- Philadelphia and Northeast regions
- Multiple additional locations nationwide
Take Action for Your Hematological Health
Don’t let uncertainty about platelet function and bleeding risks affect your quality of life. The CD36 Gene Platelet Glycoprotein IV Deficiency NGS Genetic DNA Test provides the clarity and confidence you need for proper hematological management. Our expert team is ready to guide you through the testing process and help you understand your genetic profile.
Book your CD36 genetic test today by calling our dedicated healthcare line at +1(267) 388-9828 or schedule your appointment through our online booking system. Take the first step toward comprehensive hematological health understanding with our advanced genetic testing services.
