ALPHA-1-ANTITRYPSIN AAT PHENOTYPE Test
Are you concerned about Alpha-1-Antitrypsin deficiency? DNA Labs UAE offers the ALPHA-1-ANTITRYPSIN AAT PHENOTYPE Test to help diagnose and manage this genetic disorder.
Test Cost: AED 1630.0
Wondering about the cost of the ALPHA-1-ANTITRYPSIN AAT PHENOTYPE Test? It is priced at AED 1630.0.
Symptoms and Diagnosis
Alpha-1-Antitrypsin deficiency can cause lung and liver diseases. If you experience symptoms such as chronic obstructive pulmonary disease (COPD) or liver disease, it is important to get tested. The ALPHA-1-ANTITRYPSIN AAT PHENOTYPE Test can help confirm the diagnosis and determine the severity of the deficiency.
Test Details
The ALPHA-1-ANTITRYPSIN AAT PHENOTYPE Test is a laboratory test that identifies and classifies the specific phenotype of the Alpha-1-Antitrypsin protein in your blood. This protein, produced in the liver, protects the lungs from damage caused by enzymes released by white blood cells. The test uses techniques like isoelectric focusing or polymerase chain reaction (PCR) to determine the phenotype. It can detect various phenotypes, including normal (M), deficient (Z), and other variants (S, F, etc.).
Who Should Take the Test?
If you have symptoms, a family history of Alpha-1-Antitrypsin deficiency, or abnormal lung or liver function tests, your healthcare provider may recommend the ALPHA-1-ANTITRYPSIN AAT PHENOTYPE Test. It is typically ordered by chest physicians or gastroenterologists.
Test Procedure
The ALPHA-1-ANTITRYPSIN AAT PHENOTYPE Test requires a blood sample, usually drawn from a vein in your arm. The sample is then sent to our laboratory for analysis. The results are usually available within a few days.
Report Delivery
Your sample should be sent by the 7th of the month, and the report will be delivered after 2-3 weeks.
Pre Test Information
Before taking the ALPHA-1-ANTITRYPSIN AAT PHENOTYPE Test, you must fill out the Test Send Out Consent Form. This form is mandatory.
Test Department
The ALPHA-1-ANTITRYPSIN AAT PHENOTYPE Test is conducted in the OS department of DNA Labs UAE.
Conclusion
The ALPHA-1-ANTITRYPSIN AAT PHENOTYPE Test is essential for diagnosing and managing Alpha-1-Antitrypsin deficiency. It helps confirm the diagnosis, determine the severity of the deficiency, and guide treatment decisions. By getting tested, you can receive appropriate medical interventions and genetic counseling.
| Test Name | ALPHA-1-ANTITRYPSIN AAT PHENOTYPE Test |
|---|---|
| Components | |
| Price | 1630.0 AED |
| Sample Condition | 2 mL (0.5 mL min.) serum from 1 Red Top (No Additive) tube. Do not use SST gel barrier tubes. Ship refrigerated or frozen. Duly filled Test Send Out Consent Formis mandatory. |
| Report Delivery | Sample by 7th of the month; Report after 2??3 weeks |
| Method | Isoelectrofocusing |
| Test type | Genetic Disorders |
| Doctor | Chest Physician, Gastroenterologist |
| Test Department: | OS |
| Pre Test Information | Duly filled Test Send Out Consent Formis mandatory. |
| Test Details | The Alpha-1-Antitrypsin (AAT) phenotype test is a laboratory test that determines the specific phenotype of the Alpha-1-Antitrypsin protein in an individual’s blood. Alpha-1-Antitrypsin is a protein produced in the liver that helps protect the lungs from damage caused by enzymes released by white blood cells. There are several different phenotypes of Alpha-1-Antitrypsin, including normal (M), deficient (Z), and other variants (S, F, etc.). The AAT phenotype test uses various techniques, such as isoelectric focusing or polymerase chain reaction (PCR), to identify and classify the specific phenotype of an individual. The test is primarily used to diagnose Alpha-1-Antitrypsin deficiency, a genetic disorder that increases the risk of developing lung and liver diseases. People with Alpha-1-Antitrypsin deficiency may have reduced levels or abnormal forms of the protein, which can lead to lung conditions such as chronic obstructive pulmonary disease (COPD) or liver disease. The AAT phenotype test is usually ordered by a healthcare provider if there is a suspicion of Alpha-1-Antitrypsin deficiency based on symptoms, family history, or abnormal lung or liver function tests. It can help confirm the diagnosis, determine the severity of the deficiency, and guide treatment decisions. The test requires a blood sample, which is typically drawn from a vein in the arm. The sample is then sent to a laboratory for analysis, and the results are usually available within a few days. It is important to note that the AAT phenotype test is different from the AAT level test, which measures the amount of Alpha-1-Antitrypsin protein in the blood. While the AAT level test can provide information about the quantity of the protein, the AAT phenotype test provides information about the specific genetic variants present. Overall, the AAT phenotype test plays a crucial role in diagnosing and managing Alpha-1-Antitrypsin deficiency, allowing for appropriate medical interventions and genetic counseling. |
