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Calr Mutation Detection Test

1,050 د.إ

-10%

The CALR Mutation Detection Test is a specialized diagnostic procedure aimed at identifying mutations in the calreticulin (CALR) gene. These mutations are commonly associated with certain myeloproliferative neoplasms (MPNs), including essential thrombocythemia (ET) and primary myelofibrosis (PMF). Detecting CALR mutations is crucial for the accurate diagnosis, prognosis, and treatment planning for patients affected by these conditions.

Performed at DNA Labs UAE, a leading facility in genetic testing, the CALR Mutation Detection Test employs advanced molecular techniques to ensure high sensitivity and specificity in detecting the presence of CALR gene mutations. The test is conducted by collecting a small sample of the patient’s blood or bone marrow, which is then analyzed using state-of-the-art genetic sequencing or polymerase chain reaction (PCR) methodologies.

The cost of the CALR Mutation Detection Test at DNA Labs UAE is set at 1050 AED. This price reflects the comprehensive nature of the test, including the sophisticated technology and expertise required to accurately identify CALR mutations. For patients and healthcare providers, the availability of this test represents a critical step forward in the management of MPNs, offering a clear path towards personalized treatment strategies based on genetic insights.

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CALR MUTATION DETECTION Test

At DNA Labs UAE, we offer the CALR mutation detection test to identify mutations in the CALR gene. This genetic test is commonly used in the diagnosis and management of blood disorders such as essential thrombocythemia (ET) and primary myelofibrosis (PMF).

Test Cost

The CALR mutation detection test is available at a price of AED 1050.0.

Symptoms and Diagnosis

Patients with certain blood disorders may exhibit symptoms such as abnormal bleeding, enlarged spleen, and fatigue. To diagnose these conditions, doctors may recommend the CALR mutation detection test. This test helps identify mutations in the CALR gene, which are associated with ET and PMF.

Sample Collection

To perform the CALR mutation detection test, a sample of 3 ml (minimum 2 ml) of whole blood is required. The blood should be collected in a Lavender top (EDTA) tube and shipped refrigerated. It is important not to freeze the sample. Additionally, a duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory for the test.

Report Delivery

The sample should be submitted by Monday before 11 am, and the report will be delivered on Saturday.

Method and Test Type

The CALR mutation detection test is performed using PCR (Polymerase Chain Reaction) and sequencing techniques. This test falls under the category of cancer genetic testing and is commonly requested by oncologists. It is conducted in the Molecular Diagnostics department of our lab.

Pre Test Information

Prior to the test, it is mandatory to complete the Genomics Clinical Information Requisition Form (Form 20).

Test Details

The CALR mutation detection test is specifically designed to identify mutations in the CALR gene. These mutations are associated with certain blood disorders, including ET and PMF. By analyzing a blood sample, our laboratory can detect any mutations using PCR or next-generation sequencing (NGS) techniques. The test results provide valuable information to healthcare providers, helping them diagnose and manage patients with these conditions. Additionally, the results can assist in predicting disease progression and guiding treatment decisions, ensuring personalized patient care.

Test Name CALR MUTATION DETECTION Test
Components
Price 1050.0 AED
Sample Condition 3 ml (2 ml min.) whole blood in 1 Lavender top (EDTA) tube. Ship refrigerated. DO NOT FREEZE. Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.
Report Delivery SampleMon by 11 am; Report Sat
Method PCR, Sequencing
Test type Cancer
Doctor Oncologist
Test Department: MOLECULAR DIAGNOSTICS
Pre Test Information Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.
Test Details

CALR mutation detection test is a genetic test used to identify mutations in the CALR gene. CALR gene mutations are associated with certain blood disorders, such as essential thrombocythemia (ET) and primary myelofibrosis (PMF). These mutations can help in diagnosing and monitoring these diseases.

The CALR mutation detection test is usually performed on a blood sample. The sample is analyzed in a laboratory using various techniques, such as polymerase chain reaction (PCR) or next-generation sequencing (NGS), to identify any mutations in the CALR gene.

The test results can help healthcare providers determine the presence of CALR gene mutations and their specific type. This information is crucial for diagnosing and managing patients with ET or PMF. It can also assist in predicting disease progression and guiding treatment decisions.

Overall, the CALR mutation detection test plays a significant role in the diagnosis and management of certain blood disorders, providing valuable information for personalized patient care.