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Reports Within:

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Requisites
Measures

Number of red blood cells in the blood

Identifies

Red blood cell disorders

Measures: Number of red blood cells in the blood

Identifies: Red blood cell disorders

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What is the maximum days the report can be obtained for the test

The maximum days for obtaining the report for the JAK2 Exon 14 Mutation Test is 14 days.

What are the prerequisites for the test JAK2 Exon 14 Mutation Test

  • Blood sample
  • Doctor's prescription
  • Complete blood count (CBC) test results
  • Medical history of the patient
  • Consent form signed by the patient

What are the measure values for the test JAK2 Exon 14 Mutation Test

  • Positive: Presence of JAK2 exon 14 mutation
  • Negative: Absence of JAK2 exon 14 mutation

What does this test JAK2 Exon 14 Mutation Test identify?

  • This test identifies mutations in exon 14 of the JAK2 gene.
  • Specifically, it detects mutations that are associated with myeloproliferative neoplasms, such as polycythemia vera, essential thrombocythemia, and primary myelofibrosis.
  • By identifying these mutations, the test can help diagnose and monitor these types of blood disorders.
  • Results from this test can guide treatment decisions and provide important information about disease prognosis.

Why is this test JAK2 Exon 14 Mutation Test taken?

Reason for taking JAK2 Exon 14 Mutation Test

Reason for taking JAK2 Exon 14 Mutation Test

The JAK2 Exon 14 Mutation Test is taken to detect mutations in the JAK2 gene that are associated with certain blood disorders, such as myeloproliferative neoplasms (MPNs) including polycythemia vera, essential thrombocythemia, and primary myelofibrosis.

These mutations can lead to the overproduction of blood cells, causing symptoms such as increased red blood cell count, elevated platelet count, and enlarged spleen. By identifying the presence of JAK2 exon 14 mutations, healthcare providers can accurately diagnose these conditions and develop appropriate treatment plans.

The test is typically recommended for individuals who show signs and symptoms of MPNs, such as unexplained fatigue, weakness, night sweats, and abdominal discomfort. It can also be used to monitor the response to treatment and detect disease progression.

Popular FAQs on Test

The JAK2 Exon 14 Mutation Test is a diagnostic test that detects mutations in the JAK2 gene in exon 14. Mutations in this gene can be associated with certain blood disorders, such as myeloproliferative neoplasms.
The JAK2 Exon 14 Mutation Test is performed to help diagnose or monitor certain blood disorders, such as polycythemia vera, essential thrombocythemia, and primary myelofibrosis. Detecting mutations in the JAK2 gene can help guide treatment decisions and monitor disease progression.
The JAK2 Exon 14 Mutation Test is typically performed on a blood sample. The sample is analyzed in a laboratory using techniques such as polymerase chain reaction (PCR) to detect mutations in the JAK2 gene in exon 14.
No, the JAK2 Exon 14 Mutation Test is a simple blood test and is not considered painful. Some individuals may experience mild discomfort or bruising at the site where the blood sample is taken.
The JAK2 Exon 14 Mutation Test is a low-risk procedure. Risks associated with the test are minimal and may include slight bruising or bleeding at the site where the blood sample is taken. In rare cases, there may be a risk of infection or an allergic reaction to the blood draw.

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