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Beta Thalassemia-9 Common Mutations Screening Single Test Cost

Original price was: 1,400 د.إ.Current price is: 1,050 د.إ.

-25%

The “Beta Thalassemia-9 Common Mutations Screening Single Test” is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify the presence of the most prevalent mutations associated with Beta Thalassemia. This genetic disorder is characterized by reduced production of the beta-globin chain of hemoglobin, leading to varying degrees of anemia and other health complications. The test specifically targets nine common mutations, providing a focused approach to diagnosing this condition. Priced at 1050 AED, the test offers a cost-effective solution for individuals seeking a comprehensive analysis of their genetic predisposition to Beta Thalassemia. Conducted in the advanced facilities of DNA Labs UAE, this test is a crucial tool for early detection and management of the disorder, facilitating timely interventions and informed healthcare decisions.

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  • This test is not intended for medical diagnosis or treatment
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Beta Thalassemia-9 Common Mutations screening Single Test

At DNA Labs UAE, we offer the Beta Thalassemia-9 Common Mutations screening Single Test. This test helps in diagnosing beta thalassemia and determining the specific type and severity of the condition. It is a genetic disorder characterized by reduced or absent production of beta-globin chains, leading to abnormal hemoglobin synthesis.

Test Details

The Beta Thalassemia-9 Common Mutations screening Single Test can be done with a doctor’s prescription. However, please note that the prescription is not applicable for surgery and pregnancy cases or people planning to travel abroad. The test requires a 2ml EDTA Vacutainer of peripheral blood.

The cost of the Beta Thalassemia-9 Common Mutations screening Single Test is 1050.0 AED. The test is performed using the End Point PCR method in our Genetics Test Department. The report will be delivered within 3-4 days.

Common Mutations

There are nine common mutations that are typically screened for in individuals suspected of having beta thalassemia:

  1. IVS-I-110 (G>A)
  2. IVS-I-1 (G>A)
  3. Codon 8/9 (+G)
  4. Codon 39 (C>T)
  5. Codon 41/42 (-TCTT)
  6. Codon 17 (A>T)
  7. Codon 71/72 (+A)
  8. Codon 26 (G>A)
  9. Codon 27/28 (+C)

These mutations can be detected through various molecular techniques, such as polymerase chain reaction (PCR) or DNA sequencing. Screening for these mutations helps in diagnosing beta thalassemia and determining the specific type and severity of the condition. It also aids in genetic counseling and prenatal diagnosis for families at risk of having children with beta thalassemia.

Conclusion

If you suspect that you or someone you know may have beta thalassemia, consider getting the Beta Thalassemia-9 Common Mutations screening Single Test at DNA Labs UAE. This test can provide valuable information about the condition, allowing for proper diagnosis and management. Don’t wait, get tested today!

Test Name Beta Thalassemia-9 Common Mutations screening Single Test
Components EDTA Vacutainer (2ml)
Price 1050.0 AED
Sample Condition Peripheral blood
Report Delivery 3-4 days
Method End Point PCR
Test type Genetics
Doctor General Physician
Test Department:
Pre Test Information Beta Thalassemia-9 Common Mutations screening (Single) can be done with a Doctors prescription. Prescription is not applicable for surgery and pregnancy cases or people planing to travel abroad.
Test Details

Beta thalassemia is a genetic disorder characterized by reduced or absent production of beta-globin chains, leading to abnormal hemoglobin synthesis. There are several mutations in the beta-globin gene that can cause beta thalassemia. Here are 9 common mutations that are typically screened for in individuals suspected of having beta thalassemia:

1. IVS-I-110 (G>A)

2. IVS-I-1 (G>A)

3. Codon 8/9 (+G)

4. Codon 39 (C>T)

5. Codon 41/42 (-TCTT)

6. Codon 17 (A>T)

7. Codon 71/72 (+A)

8. Codon 26 (G>A)

9. Codon 27/28 (+C)

These mutations can be detected through various molecular techniques, such as polymerase chain reaction (PCR) or DNA sequencing. Screening for these mutations helps in diagnosing beta thalassemia and determining the specific type and severity of the condition. It also aids in genetic counseling and prenatal diagnosis for families at risk of having children with beta thalassemia.

SKU: TEST-5532 Category:

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