Short Description

GATA2 Full length gene sequencing (Chronic Neutropenia, MonoMac Syndrome, Mylodysplasia, AML) is performed using Sanger Sequencing methodology. Sample that have to be given is Bone Marrow/Peripheral Blood in EDTA Vacutainer (2ml) for this test. You can expect results in 15 days

PreTest 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 planing to travel abroad.

Detail Description

GATA2 Full Length Gene Sequencing: A Breakthrough in the Diagnosis and Treatment of Chronic Neutropenia, MonoMac Syndrome, Myelodysplasia, and AML

Chronic Neutropenia, MonoMac Syndrome, Myelodysplasia, and Acute Myeloid Leukemia (AML) are life-threatening conditions that affect millions of people worldwide. These diseases are characterized by abnormal blood cell production and can lead to a range of serious health complications. However, thanks to advances in genetic testing, there is new hope for patients suffering from these conditions. GATA2 Full Length Gene Sequencing is a cutting-edge diagnostic tool that can help identify the underlying genetic cause of these diseases and provide targeted treatment options.

What is GATA2 Full Length Gene Sequencing?

GATA2 is a gene that plays a crucial role in the production of blood cells. Mutations in this gene have been linked to a range of blood disorders, including Chronic Neutropenia, MonoMac Syndrome, Myelodysplasia, and AML. GATA2 Full Length Gene Sequencing is a specialized genetic test that can identify mutations in the entire GATA2 gene. By analyzing the entire gene sequence, doctors can identify even small mutations that may be missed by other tests.

Why is GATA2 Full Length Gene Sequencing important?

GATA2 Full Length Gene Sequencing is a powerful diagnostic tool that can help doctors identify the underlying genetic cause of blood disorders. This is important for several reasons:

• Accurate diagnosis: By identifying the specific genetic mutation causing the disease, doctors can provide a more accurate diagnosis. This is important for choosing the most effective treatment options.
• Predicting disease progression: Some genetic mutations are associated with a higher risk of disease progression. By identifying these mutations, doctors can provide more targeted monitoring and treatment options.
• Familial screening: Some genetic mutations are hereditary. By identifying these mutations, doctors can provide screening options for family members who may be at risk for the same condition.

What are the symptoms of Chronic Neutropenia, MonoMac Syndrome, Myelodysplasia, and AML?

The symptoms of these diseases can vary depending on the specific condition and the severity of the disease. However, some common symptoms include:

• Frequent infections
• Fever
• Fatigue
• Bleeding or bruising easily
• Anemia
• Shortness of breath
• Unexplained weight loss
• Swollen lymph nodes

How are these diseases diagnosed?

Diagnosing these diseases typically involves a combination of blood tests, imaging tests, and bone marrow biopsies. However, these tests may not always provide a clear diagnosis. That's where GATA2 Full Length Gene Sequencing comes in. By analyzing the patient's DNA, doctors can identify the specific genetic mutation causing the disease and provide a more accurate diagnosis.

How much does GATA2 Full Length Gene Sequencing cost?

The cost of GATA2 Full Length Gene Sequencing varies depending on the specific laboratory and location. In India, DNA Labs India offers GATA2 Full Length Gene Sequencing for INR 24,000.

The Bottom Line

GATA2 Full Length Gene Sequencing is a breakthrough diagnostic tool that can help identify the underlying genetic cause of Chronic Neutropenia, MonoMac Syndrome, Myelodysplasia, and AML. By providing a more accurate diagnosis, doctors can provide more targeted treatment options and improve outcomes for patients. If you or a loved one is experiencing symptoms of these diseases, talk to your doctor about whether GATA2 Full Length Gene Sequencing may be right for you.