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Hemochromatosis HFE Full Gene Sequence Analysis Test Cost

Original price was: 9,600 د.إ.Current price is: 7,200 د.إ.

-25%

The Hemochromatosis HFE Full Gene Sequence Analysis Test is a comprehensive genetic screening designed to detect mutations in the HFE gene, which are commonly associated with hereditary hemochromatosis. Hereditary hemochromatosis is a genetic disorder that causes the body to absorb an excessive amount of iron from the diet, leading to iron overload in various organs and tissues. If left untreated, this condition can result in significant health issues, including liver disease, heart problems, diabetes, and arthritis.

The test involves analyzing the entire gene sequence of HFE to identify mutations that may predispose an individual to developing hemochromatosis. This level of analysis can provide valuable information for individuals with a family history of the condition or those exhibiting symptoms related to iron overload.

Performed at DNA Labs UAE, a facility known for its advanced genetic testing capabilities, the Hemochromatosis HFE Full Gene Sequence Analysis Test is priced at 7200 AED. The cost reflects the comprehensive nature of the test, employing cutting-edge technology to ensure accurate and reliable results. By opting for this test, individuals can gain insights into their genetic risk for hemochromatosis, enabling them to take proactive steps in managing their health in consultation with healthcare professionals.

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Hemochromatosis HFE Full Gene Sequence Analysis Test

Test Name: Hemochromatosis HFE Full Gene Sequence Analysis Test

Components: EDTA Vacutainer (2ml)

Price: 7200.0 AED

Sample Condition: Peripheral blood

Report Delivery: 4-6 weeks

Method: Sanger Sequencing

Test Type: Genetics

Doctor: Gynecologist

Test Department:

Pre Test Information: Hemochromatosis HFE Full Gene Sequence Analysis can be done with a Doctor’s prescription. Prescription is not applicable for surgery and pregnancy cases or people planning to travel abroad.

Test Details:

Hemochromatosis HFE Full Gene Sequence Analysis is a genetic test that analyzes the HFE gene for mutations that are associated with hemochromatosis. Hemochromatosis is a genetic disorder that causes the body to absorb too much iron from the diet, leading to iron overload and damage to organs such as the liver, heart, and pancreas. The HFE gene provides instructions for making a protein that helps regulate the amount of iron in the body. Mutations in the HFE gene can disrupt this process, leading to excessive iron absorption and accumulation in the body.

The Hemochromatosis HFE Full Gene Sequence Analysis test involves sequencing the entire HFE gene to identify any mutations or variants that may be associated with hemochromatosis. This test can help diagnose hemochromatosis and identify individuals who may be at risk for developing the condition. The test is typically performed on a blood or saliva sample, and results are usually available within a few weeks.

Treatment for hemochromatosis typically involves regular blood removal (phlebotomy) to reduce iron levels in the body. Early diagnosis and treatment can help prevent serious complications of hemochromatosis.

Test Name Hemochromatosis HFE Full Gene Sequence Analysis Test
Components EDTA Vacutainer (2ml)
Price 7200.0 AED
Sample Condition Peipheral blood
Report Delivery 4-6 weeks
Method Sanger Sequencing
Test type Genetics
Doctor Gynecologist
Test Department:
Pre Test Information Hemochromatosis HFE Full Gene Sequence Analysis can be done with a Doctors prescription. Prescription is not applicable for surgery and pregnancy cases or people planing to travel abroad.
Test Details

Hemochromatosis HFE Full Gene Sequence Analysis is a genetic test that analyzes the HFE gene for mutations that are associated with hemochromatosis. Hemochromatosis is a genetic disorder that causes the body to absorb too much iron from the diet, leading to iron overload and damage to organs such as the liver, heart, and pancreas.

The HFE gene provides instructions for making a protein that helps regulate the amount of iron in the body. Mutations in the HFE gene can disrupt this process, leading to excessive iron absorption and accumulation in the body.

The Hemochromatosis HFE Full Gene Sequence Analysis test involves sequencing the entire HFE gene to identify any mutations or variants that may be associated with hemochromatosis. This test can help diagnose hemochromatosis and identify individuals who may be at risk for developing the condition.

The test is typically performed on a blood or saliva sample, and results are usually available within a few weeks. Treatment for hemochromatosis typically involves regular blood removal (phlebotomy) to reduce iron levels in the body. Early diagnosis and treatment can help prevent serious complications of hemochromatosis.