RUNX1 Gene Platelet Disorder With Associated Myeloid Malignancy NGS Genetic DNA Test
Introduction
The RUNX1 Gene Platelet Disorder with Associated Myeloid Malignancy NGS Genetic DNA Test is a specialized diagnostic test that examines genetic mutations in the RUNX1 gene, which are linked to various hematological disorders, particularly those affecting platelet function and myeloid malignancies. Understanding these genetic factors is crucial for effective diagnosis and treatment.
What the Test Measures
This test measures the presence of mutations in the RUNX1 gene, which can lead to platelet disorders and increase the risk of developing myeloid malignancies such as acute myeloid leukemia (AML). By utilizing Next-Generation Sequencing (NGS) technology, the test provides comprehensive insights into the genetic makeup of an individual’s blood cells.
Who Should Consider This Test
Individuals experiencing symptoms such as unexplained bleeding, easy bruising, or a family history of platelet disorders or myeloid malignancies should consider this test. Risk factors include:
- Family history of RUNX1 gene mutations
- Previous diagnosis of hematological disorders
- Symptoms indicating platelet dysfunction
Benefits of Taking the Test
- Accurate identification of genetic mutations associated with platelet disorders.
- Informed decision-making regarding treatment options.
- Early detection of potential malignancies, leading to timely intervention.
- Personalized medicine approach based on genetic findings.
Understanding Your Results
Results from the RUNX1 Gene Platelet Disorder NGS Genetic DNA Test will provide insights into the presence of genetic mutations. It is important to discuss these results with a qualified healthcare professional, such as a hematologist or genetic counselor, to understand their implications and plan appropriate management strategies.
Test Pricing
Test Name | Discount Price | Regular Price |
---|---|---|
RUNX1 Gene Platelet Disorder NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
Branches and Booking Information
We have branches across all major cities in Kenya, ensuring accessibility to our services. For your convenience, we also offer home sample collection services. To book the RUNX1 Gene Platelet Disorder with Associated Myeloid Malignancy NGS Genetic DNA Test, please contact us via phone or WhatsApp at +254713408028.
Pre-Test Instructions
A clinical history of the patient is required prior to undergoing the RUNX1 Gene Platelet Disorder with Associated Myeloid Malignancy NGS Genetic DNA Test. Additionally, a genetic counseling session is recommended to draw a pedigree chart of family members affected by the RUNX1 gene mutations.
With a turnaround time of 3 to 4 weeks, this test is essential for those at risk of hereditary platelet disorders and associated malignancies. Don’t wait—book your test today!