ATP1A3 Gene DYT12 Genetic Test
Components: ATP1A3 Gene DYT12 Genetic Test
Price: 4400.0 AED
Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery: 3 to 4 Weeks
Method: NGS Technology
Test Type: Neurological Disorders
Doctor: Neurologist
Test Department: Genetics
Pre Test Information: Clinical History of Patient who is going for ATP1A3 Gene DYT12 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ATP1A3 Gene DYT12.
Test Details
The ATP1A3 gene is associated with DYT12, a rare genetic disorder that affects movement and muscle control. The ATP1A3 gene provides instructions for making a protein called sodium/potassium-transporting ATPase subunit alpha-3, which is involved in the movement of ions across cell membranes.
The NGS (next-generation sequencing) genetic test for DYT12 involves analyzing the DNA sequence of the ATP1A3 gene to look for mutations or variations that may be associated with the disorder. This test can help diagnose DYT12 in individuals who have symptoms of the disorder, as well as identify carriers of the gene mutation in families with a history of DYT12.
Symptoms of DYT12 can include involuntary muscle movements (dystonia), difficulty with coordination and balance, tremors, and other movement disorders. The severity of symptoms can vary widely, even among individuals with the same genetic mutation.
There is currently no cure for DYT12, but treatments such as medications and physical therapy can help manage symptoms and improve quality of life for affected individuals. Genetic testing can also provide important information for family planning and genetic counseling.
| Test Name | ATP1A3 Gene DYT12 Genetic Test |
|---|---|
| Components | |
| Price | 4400.0 AED |
| Sample Condition | Blood or Extracted DNA or One drop Blood on FTA Card o |
| Report Delivery | 3 to 4 Weeks |
| Method | NGS Technology |
| Test type | Neurological Disorders |
| Doctor | Neurologist |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for ATP1A3 Gene DYT12 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with ATP1A3 Gene DYT12 |
| Test Details | The ATP1A3 gene is associated with DYT12, a rare genetic disorder that affects movement and muscle control. The ATP1A3 gene provides instructions for making a protein called sodium/potassium-transporting ATPase subunit alpha-3, which is involved in the movement of ions across cell membranes. The NGS (next-generation sequencing) genetic test for DYT12 involves analyzing the DNA sequence of the ATP1A3 gene to look for mutations or variations that may be associated with the disorder. This test can help diagnose DYT12 in individuals who have symptoms of the disorder, as well as identify carriers of the gene mutation in families with a history of DYT12. Symptoms of DYT12 can include involuntary muscle movements (dystonia), difficulty with coordination and balance, tremors, and other movement disorders. The severity of symptoms can vary widely, even among individuals with the same genetic mutation. There is currently no cure for DYT12, but treatments such as medications and physical therapy can help manage symptoms and improve quality of life for affected individuals. Genetic testing can also provide important information for family planning and genetic counseling. |
