Huntington Disease HD Mutation Screening Test
At DNA Labs UAE, we offer the Huntington Disease HD mutation screening test for individuals who suspect they may be at risk of developing Huntington’s disease. This genetic test is designed to detect the presence of the mutation responsible for the disease.
Test Details
The Huntington Disease HD mutation screening test involves analyzing a person’s DNA to identify the specific mutation in the huntingtin (HTT) gene. This can be done through various techniques such as polymerase chain reaction (PCR), DNA sequencing, or other molecular genetic methods.
The test is typically performed on individuals who have a family history of Huntington’s disease or who are showing symptoms consistent with the disease. It can also be used for prenatal testing in cases where there is a known family history of HD.
The presence of the HD mutation indicates that an individual is at risk of developing Huntington’s disease. However, it is important to note that not everyone who carries the mutation will develop the disease, as there is variability in the age of onset and severity of symptoms.
Test Components
- EDTA Vacutainer (2ml)
Price
The cost of the Huntington Disease HD mutation screening test is 1600.0 AED.
Sample Condition
The test requires a peripheral blood sample.
Report Delivery
Once the sample is received, the test results will be delivered within 3-4 days.
Method
The Huntington Disease HD mutation screening test is conducted using the End Point PCR method.
Test Type
The test falls under the category of Genetics.
Referring Doctor
A General Physician can refer you for the Huntington Disease HD mutation screening test.
Test Department
This test is conducted in our Genetics department.
Pre Test Information
Please note that a doctor’s prescription is required for the Huntington Disease HD mutation screening test. However, this prescription is not applicable for surgery and pregnancy cases or individuals planning to travel abroad.
Genetic Counseling
Before and after undergoing the Huntington Disease HD mutation screening test, it is highly recommended to seek genetic counseling. This will help you understand the implications of the test results and make informed decisions about your health and future planning.
| Test Name | Huntington Disease HD mutation screening Test |
|---|---|
| Components | EDTA Vacutainer (2ml) |
| Price | 1600.0 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 | Huntington Disease (HD) mutation screening can be done with a Doctors prescription. Prescription is not applicable for surgery and pregnancy cases or people planing to travel abroad. |
| Test Details |
Huntington’s disease (HD) mutation screening is a genetic test that is used to detect the presence of the mutation responsible for Huntington’s disease. HD is a neurodegenerative disorder that is caused by a mutation in the huntingtin (HTT) gene. The HD mutation screening test involves analyzing a person’s DNA to identify the specific mutation in the HTT gene. This can be done through various techniques such as polymerase chain reaction (PCR), DNA sequencing, or other molecular genetic methods. The test is typically performed on individuals who have a family history of HD or who are showing symptoms consistent with the disease. It can also be used for prenatal testing in cases where there is a known family history of HD. The presence of the HD mutation indicates that an individual is at risk of developing Huntington’s disease. However, it is important to note that not everyone who carries the mutation will develop the disease, as there is variability in the age of onset and severity of symptoms. Genetic counseling is usually recommended before and after HD mutation screening to help individuals understand the implications of the test results and make informed decisions about their health and future planning. |
