Hereditary Spastic Paraplegia Gene Panel Test
Components: Sterile container/ Sterile Normal Saline Container/ EDTA Vacutainer
Price: 7200.0 AED
Sample Condition: Amniotic fluid/ Chorionic villi/ Peripheral blood
Report Delivery: 4-6 weeks
Method: NGS (Next Generation Sequencing)
Test Type: Genetics
Doctor: General Physician
Test Department: DNA Labs UAE
Pre Test Information: Hereditary Spastic Paraplegia Gene Panel can be done with a doctor’s prescription. Prescription is not applicable for surgery and pregnancy cases or people planning to travel abroad.
Test Details:
A Hereditary Spastic Paraplegia (HSP) gene panel is a genetic test that analyzes a set of genes associated with HSP, a group of rare inherited neurological disorders that affect the lower limbs. The panel typically includes more than 80 genes that have been linked to different types of HSP.
The test is usually performed using a small blood sample or saliva sample and can help diagnose the specific type of HSP in a patient, which can guide treatment and management strategies. The test may also be used for carrier testing or prenatal diagnosis in families with a known HSP mutation.
Test Name | Hereditary Spastic Paraplegia Gene Panel Test |
---|---|
Components | Sterile container/ Sterile Normal Saline Container/ EDTA Vacutainer |
Price | 7200.0 AED |
Sample Condition | Amniotic fluid\/ Chorionic villi\/ Peripheral blood |
Report Delivery | 4-6 weeks |
Method | NGS |
Test type | Genetics |
Doctor | General Physician |
Test Department: | |
Pre Test Information | Hereditary Spastic Paraplegia Gene Panel can be done with a Doctors prescription. Prescription is not applicable for surgery and pregnancy cases or people planing to travel abroad. |
Test Details |
A Hereditary Spastic Paraplegia (HSP) gene panel is a genetic test that analyzes a set of genes associated with HSP, a group of rare inherited neurological disorders that affect the lower limbs. The panel typically includes more than 80 genes that have been linked to different types of HSP. The test is usually performed using a small blood sample or saliva sample and can help diagnose the specific type of HSP in a patient, which can guide treatment and management strategies. The test may also be used for carrier testing or prenatal diagnosis in families with a known HSP mutation. |