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GATA2 Full-Length Gene Sequencing Chronic Neutropenia MonoMac Syndrome Mylodysplasia AML Test

2,800 د.إ

-56%

The “GATA2 Full-Length Gene Sequencing Test” is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the GATA2 gene, which are associated with a spectrum of hematologic conditions and disorders. This gene plays a crucial role in the development and function of the immune system, and mutations can lead to conditions such as chronic neutropenia, MonoMac syndrome, myelodysplastic syndromes (MDS), and acute myeloid leukemia (AML). These disorders are characterized by a range of symptoms, including increased susceptibility to infections, anemia, and a higher risk of developing leukemia.

The test, priced at 2800 AED, involves sequencing the entire length of the GATA2 gene to pinpoint specific genetic alterations. This comprehensive approach ensures a high level of accuracy in diagnosis, which is critical for the effective management and treatment of the associated conditions. Early detection through this genetic testing allows for timely intervention, potentially improving patient outcomes.

Performed at the state-of-the-art facilities of DNA Labs UAE, the test is conducted under stringent quality controls, ensuring reliable and precise results. For individuals presenting symptoms indicative of the related disorders, or those with a family history of such conditions, the GATA2 Full-Length Gene Sequencing Test offers a valuable diagnostic tool, aiding in the development of personalized treatment plans.

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GATA2 Full Length Gene Sequencing – Chronic Neutropenia MonoMac Syndrome Mylodysplasia AML Test

Test Details

GATA2 is a transcription factor that plays a critical role in the development and function of hematopoietic cells, including neutrophils, monocytes, and dendritic cells. Mutations in the GATA2 gene have been associated with a range of hematological disorders, including chronic neutropenia, MonoMac syndrome, myelodysplasia, and acute myeloid leukemia (AML).

Full-length gene sequencing of GATA2 can help identify mutations or variants that may be contributing to these disorders. This involves sequencing the entire coding region of the GATA2 gene, as well as its promoter and other regulatory regions, to identify any changes in the DNA sequence that may be causing functional changes in the protein.

In patients with chronic neutropenia, GATA2 mutations may lead to a reduction in the number of circulating neutrophils, which can increase the risk of infections. MonoMac syndrome is characterized by a lack of monocytes and dendritic cells, which can lead to recurrent infections and other immune system abnormalities. Myelodysplasia is a disorder of the bone marrow in which immature blood cells fail to mature properly, leading to anemia, infections, and other complications. AML is a type of blood cancer that can develop from abnormal blood stem cells and can be associated with GATA2 mutations.

Identifying GATA2 mutations through full-length gene sequencing can help clinicians better understand the underlying causes of these disorders and develop targeted treatment strategies.

Test Name

GATA2 Full Length Gene Sequencing Chronic Neutropenia MonoMac Syndrome Mylodysplasia AML Test

Components

  • EDTA Vacutainer (2ml)

Price

2800.0 AED

Sample Condition

Bone Marrow/Peripheral Blood

Report Delivery

15 days

Method

Sanger Sequencing

Test Type

Genetics

Doctor

Gynecologist

Test Department

Pre Test Information

Pre Test Information

GATA2 Full Length Gene Sequencing (Chronic Neutropenia, MonoMac Syndrome, Mylodysplasia, AML) can be done with a doctor’s prescription. Prescription is not applicable for surgery and pregnancy cases or people planning to travel abroad.

Test Name GATA2 Full length gene sequencing Chronic Neutropenia MonoMac Syndrome Mylodysplasia AML Test
Components EDTA Vacutainer (2ml)
Price 2800.0 AED
Sample Condition Bone Marrow\/Peripheral Blood
Report Delivery 15 days
Method Sanger Sequencing
Test type Genetics
Doctor Gynecologist
Test Department:
Pre Test Information GATA2 Full length gene sequencing (Chronic Neutropenia, MonoMac Syndrome, Mylodysplasia, AML) can be done with a Doctors prescription. Prescription is not applicable for surgery and pregnancy cases or people planing to travel abroad.
Test Details

GATA2 is a transcription factor that plays a critical role in the development and function of hematopoietic cells, including neutrophils, monocytes, and dendritic cells. Mutations in the GATA2 gene have been associated with a range of hematological disorders, including chronic neutropenia, MonoMac syndrome, myelodysplasia, and acute myeloid leukemia (AML).

Full-length gene sequencing of GATA2 can help identify mutations or variants that may be contributing to these disorders. This involves sequencing the entire coding region of the GATA2 gene, as well as its promoter and other regulatory regions, to identify any changes in the DNA sequence that may be causing functional changes in the protein.

In patients with chronic neutropenia, GATA2 mutations may lead to a reduction in the number of circulating neutrophils, which can increase the risk of infections. MonoMac syndrome is characterized by a lack of monocytes and dendritic cells, which can lead to recurrent infections and other immune system abnormalities. Myelodysplasia is a disorder of the bone marrow in which immature blood cells fail to mature properly, leading to anemia, infections, and other complications. AML is a type of blood cancer that can develop from abnormal blood stem cells and can be associated with GATA2 mutations.

Identifying GATA2 mutations through full-length gene sequencing can help clinicians better understand the underlying causes of these disorders and develop targeted treatment strategies.

SKU: TEST-810 Category:

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