CALR Mutation Analysis Deletion or Insertion in Exon 9
Introduction to CALR Mutation Analysis
The CALR Mutation Analysis Deletion or Insertion in Exon 9 is a specialized genetic test that plays a vital role in diagnosing certain blood disorders such as myeloproliferative neoplasms (MPNs). This test is essential for understanding the underlying genetic factors that contribute to these conditions, enabling healthcare providers to tailor treatment plans effectively.
What the Test Measures
This test specifically detects mutations in the CALR gene, which are known to be associated with various hematological disorders. By analyzing the presence of deletions or insertions in Exon 9 of the CALR gene, clinicians can gain insights into the genetic predispositions of patients.
Who Should Consider This Test?
Individuals who may benefit from CALR Mutation Analysis include:
- Patients experiencing unexplained symptoms such as fatigue, night sweats, or unexplained weight loss.
- Individuals with a family history of blood disorders.
- Patients diagnosed with conditions like essential thrombocythemia or primary myelofibrosis.
Benefits of Taking the Test
Undergoing the CALR Mutation Analysis offers several benefits, including:
- Accurate diagnosis of genetic conditions.
- Guidance for treatment options based on genetic findings.
- Informed decision-making for patients and their families regarding health management.
Understanding Your Results
Results from the CALR Mutation Analysis will provide insight into whether a mutation is present. A positive result may indicate a higher risk for certain blood disorders, while a negative result can help rule out these conditions. It is essential to discuss your results with a healthcare professional for proper interpretation and guidance.
Test Details and Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| CALR Mutation Analysis Deletion or Insertion in Exon 9 | 180000 NGN | 240000 NGN |
Booking Your Test
To schedule your CALR Mutation Analysis, please contact us at +2348077798758. Our team is ready to assist you in booking your test and answering any questions you may have.
Additional Information
Turnaround time for results is approximately 7-8 days. The sample type required for this test is either bone marrow or peripheral blood, collected in an EDTA Vacutainer (2ml). Please note that a Doctor’s prescription is required for this test, except in cases of surgery, pregnancy, or international travel.
