TP63 Gene Limb-Mammary Syndrome NGS Genetic DNA Test
The TP63 Gene Limb-Mammary Syndrome NGS Genetic DNA Test is a cutting-edge diagnostic tool that utilizes Next Generation Sequencing (NGS) technology to analyze the TP63 gene. This test is crucial for identifying genetic mutations linked to limb-mammary syndrome, a rare condition characterized by developmental anomalies affecting the limbs and mammary glands.
Importance of the TP63 Gene Test
This test plays a vital role in the early diagnosis and management of limb-mammary syndrome, enabling healthcare providers to offer tailored treatment plans for affected individuals. Understanding genetic predispositions can significantly improve patient outcomes.
What the Test Measures
The TP63 Gene Limb-Mammary Syndrome NGS Genetic DNA Test detects mutations in the TP63 gene, which are associated with various developmental disorders. By identifying these mutations, clinicians can better understand the genetic basis of the patient’s condition.
Who Should Consider This Test?
This test is recommended for individuals displaying symptoms of limb-mammary syndrome, such as:
- Abnormal limb development
- Breast development issues
- Family history of limb-mammary syndrome or other genetic disorders
- Patients seeking genetic counseling for reproductive planning
Benefits of Taking the Test
- Early diagnosis of genetic conditions
- Informed decision-making for treatment options
- Family planning guidance based on genetic risks
- Access to specialized care and resources
Understanding Your Results
Results from the TP63 Gene Limb-Mammary Syndrome NGS Genetic DNA Test will provide insights into whether a mutation in the TP63 gene is present. A genetic counselor will help interpret these results, explaining their implications for the patient and their family.
Test Details
Test Name | Discount Price | Regular Price |
---|---|---|
TP63 Gene Limb-Mammary Syndrome NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Booking Your Test
To book the TP63 Gene Limb-Mammary Syndrome NGS Genetic DNA Test, please call or WhatsApp us at +2348077798758. Our team is ready to assist you with the booking process and answer any questions you may have.
Pre-Test Instructions
Before undergoing the test, patients are advised to provide a detailed clinical history. A genetic counseling session is recommended to draw a pedigree chart of family members affected by the TP63 gene mutations. Sample types accepted include blood, extracted DNA, or one drop of blood on an FTA card.
Turnaround Time: 3 to 4 Weeks
Specialty: Pediatrics
Department: Genetics
Method: NGS Technology
Disease Type: Dysmorphology