G6PD Gene Mutation Detection Test
Are you experiencing symptoms of G6PD deficiency? Get the G6PD Gene Mutation Detection Test at DNA Labs UAE for only 990.0 AED!
Test Details
The G6PD gene mutation detection test is a laboratory test that is used to identify mutations in the glucose-6-phosphate dehydrogenase (G6PD) gene. This gene provides instructions for producing an enzyme called glucose-6-phosphate dehydrogenase, which is important for the normal function of red blood cells.
Mutations in the G6PD gene can lead to a deficiency in the glucose-6-phosphate dehydrogenase enzyme. This deficiency can cause a condition called G6PD deficiency, which is characterized by the inability of red blood cells to properly protect themselves against oxidative stress. This can result in the destruction of red blood cells, leading to a condition known as hemolytic anemia.
The G6PD gene mutation detection test involves analyzing a sample of blood or DNA to identify any mutations or variations in the G6PD gene. This can be done using various techniques, such as polymerase chain reaction (PCR) or DNA sequencing. The test can detect specific mutations that are known to be associated with G6PD deficiency.
Test Information
- Test Name: G6PD Gene Mutation Detection Test
- Components: PCR
- Price: 990.0 AED
- Sample Condition: 4 mL (2 mL min.) whole blood in 1 Lavender top (EDTA) tube. Ship refrigerated. DO NOT FREEZE.
- Report Delivery: SampleMon by 11 am; Report 10 days
- Test Type: Genetic Disorders
- Doctor: Physician, Hematologist
- Test Department: MOLECULAR DIAGNOSTICS
- Pre Test Information: Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.
Why Should You Get Tested?
The G6PD gene mutation detection test is typically performed when a person has symptoms or a family history that suggests G6PD deficiency. It can also be used for screening purposes in certain populations or before administering medications that may cause oxidative stress, as individuals with G6PD deficiency may be at risk for severe adverse reactions.
The results of the test can help in confirming a diagnosis of G6PD deficiency and determining the specific mutation present. This information can be important for guiding treatment decisions and managing the condition.
It is important to note that the G6PD gene mutation detection test is a specialized test that is typically performed in a laboratory setting by trained professionals. It is not a routine test and may not be available in all healthcare facilities. A healthcare provider can provide more information on whether the test is appropriate and available in a specific situation.
| Test Name | G6PD GENE MUTATION DETECTION Test |
|---|---|
| Components | |
| Price | 990.0 AED |
| Sample Condition | 4 mL (2 mL min.) whole blood in 1 Lavender top (EDTA) tube. Ship refrigerated. DO NOT FREEZE. Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory. |
| Report Delivery | SampleMon by 11 am; Report 10 days |
| Method | PCR |
| Test type | Genetic Disorders |
| Doctor | Physician, Hematologist |
| Test Department: | MOLECULAR DIAGNOSTICS |
| Pre Test Information | Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory. |
| Test Details | The G6PD gene mutation detection test is a laboratory test that is used to identify mutations in the glucose-6-phosphate dehydrogenase (G6PD) gene. This gene provides instructions for producing an enzyme called glucose-6-phosphate dehydrogenase, which is important for the normal function of red blood cells. Mutations in the G6PD gene can lead to a deficiency in the glucose-6-phosphate dehydrogenase enzyme. This deficiency can cause a condition called G6PD deficiency, which is characterized by the inability of red blood cells to properly protect themselves against oxidative stress. This can result in the destruction of red blood cells, leading to a condition known as hemolytic anemia. The G6PD gene mutation detection test involves analyzing a sample of blood or DNA to identify any mutations or variations in the G6PD gene. This can be done using various techniques, such as polymerase chain reaction (PCR) or DNA sequencing. The test can detect specific mutations that are known to be associated with G6PD deficiency. The G6PD gene mutation detection test is typically performed when a person has symptoms or a family history that suggests G6PD deficiency. It can also be used for screening purposes in certain populations or before administering medications that may cause oxidative stress, as individuals with G6PD deficiency may be at risk for severe adverse reactions. The results of the test can help in confirming a diagnosis of G6PD deficiency and determining the specific mutation present. This information can be important for guiding treatment decisions and managing the condition. It is important to note that the G6PD gene mutation detection test is a specialized test that is typically performed in a laboratory setting by trained professionals. It is not a routine test and may not be available in all healthcare facilities. A healthcare provider can provide more information on whether the test is appropriate and available in a specific situation. |
