Sickle Cell Anemia Mutation Detection Test
Are you concerned about sickle cell anemia? DNA Labs UAE offers the Sickle Cell Anemia Mutation Detection test to help diagnose this genetic disorder. Read on to learn more about the test, its cost, symptoms, diagnosis, and more.
Test Details
The Sickle Cell Anemia Mutation Detection test is a diagnostic test used to detect mutations in the gene responsible for sickle cell anemia. Sickle cell anemia is a genetic disorder characterized by the presence of abnormal hemoglobin, which leads to the production of sickle-shaped red blood cells.
Test Components
- HBB
Test Cost
The cost of the Sickle Cell Anemia Mutation Detection test is AED 700.0.
Sample Condition
A minimum of 2 mL and a maximum of 4 mL of whole blood from 1 Lavender Top (EDTA) tube is required for the test. The sample should be shipped refrigerated and should not be frozen. Additionally, a duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.
Report Delivery
The sample should be submitted by Monday 11 am, and the report will be delivered on Friday.
Method
The Sickle Cell Anemia Mutation Detection test uses PCR (Polymerase Chain Reaction) and Sequencing methods for analysis.
Test Type
The Sickle Cell Anemia Mutation Detection test specifically targets sickle cell anemia.
Doctor
The test is performed under the supervision of a physician or hematologist.
Test Department
The Sickle Cell Anemia Mutation Detection test is conducted in the Molecular Diagnostics department.
Pre Test Information
A duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory before undergoing the test.
Symptoms and Diagnosis
Sickle cell anemia can cause a variety of symptoms, including fatigue, jaundice, pain crises, and increased susceptibility to infections. Diagnosis of sickle cell anemia is confirmed through genetic testing, such as the Sickle Cell Anemia Mutation Detection test.
Carrier Testing
The Sickle Cell Anemia Mutation Detection test can also be used for carrier testing. This is particularly important for individuals with a family history of sickle cell anemia, as they may be at risk of passing the mutation on to their children.
Importance of Early Detection
Early detection of the sickle cell anemia mutation is crucial for appropriate management and treatment of the condition. It allows for early intervention and monitoring to prevent complications associated with the disease, such as pain crises, organ damage, and infections.
Treatment and Genetic Counseling
It is important to note that the Sickle Cell Anemia Mutation Detection test is not a cure for sickle cell anemia. However, it provides valuable information for healthcare providers to develop an appropriate treatment plan and offer genetic counseling to affected individuals and their families.
If you suspect you or a loved one may have sickle cell anemia, don’t hesitate to contact DNA Labs UAE for the Sickle Cell Anemia Mutation Detection test. Early detection can make a significant difference in managing this genetic disorder.
| Test Name | SICKLE CELL ANEMIA MUTATION DETECTION Test |
|---|---|
| Components | *HBB |
| Price | 700.0 AED |
| Sample Condition | 4 mL (2 mL min.) whole blood from 1 LavenderTop(EDTA)tube. Ship refrigerated. DO NOT FREEZE.DO NOT FREEZE. Duly filledGenomics Clinical information requisition form (Form 20) is mandatory. |
| Report Delivery | SampleMon by 11 am; Report Fri |
| Method | PCR, Sequencing |
| Test type | Sickle cell anemia |
| Doctor | Physician, Hematologist |
| Test Department: | MOLECULAR DIAGNOSTICS |
| Pre Test Information | Duly filledGenomics Clinical information requisition form (Form 20) is mandatory. |
| Test Details |
The Sickle Cell Anemia Mutation Detection test is a diagnostic test used to detect mutations in the gene responsible for sickle cell anemia. Sickle cell anemia is a genetic disorder characterized by the presence of abnormal hemoglobin, which leads to the production of sickle-shaped red blood cells. The test typically involves a blood sample from the patient, which is then analyzed in a laboratory. There are several different methods used to detect the specific mutation responsible for sickle cell anemia, including DNA sequencing, polymerase chain reaction (PCR), and restriction fragment length polymorphism (RFLP) analysis. The test can identify the specific mutation in the gene that causes sickle cell anemia, allowing for a definitive diagnosis. It can also be used for carrier testing, which is important for individuals with a family history of sickle cell anemia who may be at risk of passing the mutation on to their children. Early detection of the sickle cell anemia mutation is crucial for appropriate management and treatment of the condition. It allows for early intervention and monitoring to prevent complications associated with the disease, such as pain crises, organ damage, and infections. It is important to note that the Sickle Cell Anemia Mutation Detection test is not a cure for sickle cell anemia. However, it provides valuable information for healthcare providers to develop an appropriate treatment plan and offer genetic counseling to affected individuals and their families. |
