THALASSEMIA ALPHA MUTATION ANALYSIS Test
Test Cost: AED 940.0
Symptoms, Diagnosis, and Test Details
The Thalassemia Alpha Mutation Analysis test is a genetic test used to detect mutations in the alpha globin genes, which are responsible for the production of alpha globin chains in hemoglobin. Thalassemia is a group of inherited blood disorders characterized by abnormal hemoglobin production, leading to reduced red blood cell production and anemia.
This test specifically focuses on mutations in the alpha globin genes, as mutations in these genes can result in alpha thalassemia, a type of thalassemia characterized by reduced or absent production of alpha globin chains. Alpha thalassemia can range from mild to severe, depending on the number and type of mutations present.
The Thalassemia Alpha Mutation Analysis test typically involves analyzing a blood sample to identify specific mutations in the alpha globin genes. This can be done through various techniques, such as DNA sequencing or polymerase chain reaction (PCR).
The results of the test can help diagnose alpha thalassemia and determine its severity. They can also provide valuable information for genetic counseling and family planning, as alpha thalassemia is an inherited condition.
It is important to note that this test specifically targets mutations in the alpha globin genes and may not detect mutations in other genes associated with thalassemia, such as the beta globin genes. Additional tests may be necessary to fully evaluate a person’s thalassemia status.
Test Components:
- Price: AED 940.0
- Sample Condition: 4 mL (2 mL min.) whole blood from 1 Lavender Top (EDTA) tube. Ship refrigerated. DO NOT FREEZE.
- Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.
Report Delivery:
Sample collected on Monday by 9 am; Report delivered on Friday.
Method:
PCR, MLPA
Test Type:
Genetic Disorders
Doctor:
Hematologist
Test Department:
Molecular Diagnostics
Pre Test Information:
Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.
Test Name | THALASSEMIA ALPHA MUTATION ANALYSIS Test |
---|---|
Components | |
Price | 940.0 AED |
Sample Condition | 4 mL (2 mL min.) whole blood from 1 Lavender Top (EDTA) tube. Ship refrigerated. DO NOT FREEZE. Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory. |
Report Delivery | Sample Mon by 9 am; Report Fri |
Method | PCR, MLPA |
Test type | Genetic Disorders |
Doctor | Hematologist |
Test Department: | MOLECULAR DIAGNOSTICS |
Pre Test Information | Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory. |
Test Details |
The Thalassemia Alpha Mutation Analysis test is a genetic test used to detect mutations in the alpha globin genes, which are responsible for the production of alpha globin chains in hemoglobin. Thalassemia is a group of inherited blood disorders characterized by abnormal hemoglobin production, leading to reduced red blood cell production and anemia. This test specifically focuses on mutations in the alpha globin genes, as mutations in these genes can result in alpha thalassemia, a type of thalassemia characterized by reduced or absent production of alpha globin chains. Alpha thalassemia can range from mild to severe, depending on the number and type of mutations present. The Thalassemia Alpha Mutation Analysis test typically involves analyzing a blood sample to identify specific mutations in the alpha globin genes. This can be done through various techniques, such as DNA sequencing or polymerase chain reaction (PCR). The results of the test can help diagnose alpha thalassemia and determine its severity. They can also provide valuable information for genetic counseling and family planning, as alpha thalassemia is an inherited condition. It is important to note that this test specifically targets mutations in the alpha globin genes and may not detect mutations in other genes associated with thalassemia, such as the beta globin genes. Additional tests may be necessary to fully evaluate a person’s thalassemia status. |