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ATP1A3 Gene DYT12 Genetic Test

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The ATP1A3 gene DYT12 genetic test is a specialized diagnostic tool designed to identify mutations in the ATP1A3 gene, which are linked to DYT12, also known as Rapid-Onset Dystonia-Parkinsonism. This condition is characterized by the sudden development of dystonia—a disorder that causes involuntary muscle contractions, leading to abnormal postures and movements—accompanied by symptoms of Parkinsonism such as tremors, bradykinesia, and rigidity. The test plays a crucial role in the accurate diagnosis and management of the condition, enabling healthcare providers to tailor treatment plans effectively.

Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, the test involves analyzing the patient’s DNA to detect any abnormalities or mutations in the ATP1A3 gene. The process is known for its accuracy and reliability, making it a valuable asset in the field of medical genetics.

The cost of the ATP1A3 gene DYT12 genetic test at DNA Labs UAE is set at 4400 AED. While the price may seem high, the test offers invaluable insights into the genetic underpinnings of DYT12, facilitating early intervention and potentially improving the quality of life for those affected by this rare condition.

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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.