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SLC6A3 Gene Parkinsonism-Dystonia Infantile Genetic Test Cost

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

-21%

The SLC6A3 gene Parkinsonism-Dystonia Infantile genetic test is a specialized diagnostic tool designed to detect mutations in the SLC6A3 gene, which have been associated with the development of Parkinsonism-Dystonia in infancy. This rare genetic disorder is characterized by a combination of Parkinsonian symptoms such as tremors, rigidity, and bradykinesia, alongside dystonia, which involves involuntary muscle contractions leading to abnormal postures or movements. Early detection through genetic testing can be crucial for managing symptoms and improving the quality of life for affected individuals.

Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, the test offers a comprehensive analysis of the SLC6A3 gene to identify any mutations that may be present. The process involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed using advanced genetic sequencing technologies.

The cost of the SLC6A3 gene Parkinsonism-Dystonia Infantile genetic test is 4400 AED. While the price may seem significant, the value of early and accurate diagnosis cannot be overstated, as it opens the door to targeted treatments and interventions that can significantly benefit the patient. Individuals with a family history of Parkinsonism-Dystonia or those showing early symptoms of the disorder are encouraged to consider this test. It’s also advisable to consult with a healthcare provider or a genetic counselor to understand the implications of the test results fully.

Description

SLC6A3 Gene Parkinsonism-Dystonia infantile Genetic Test

Components: SLC6A3 Gene Parkinsonism-Dystonia infantile 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 SLC6A3 Gene Parkinsonism-Dystonia, infantile NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SLC6A3 Gene Parkinsonism-Dystonia, infantile

Test Details:

The SLC6A3 gene is associated with a condition called Parkinsonism-Dystonia, infantile. This is a genetic disorder characterized by the combination of parkinsonism (movement problems similar to Parkinson’s disease) and dystonia (involuntary muscle contractions).

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses high-throughput sequencing technologies to analyze multiple genes simultaneously. In the context of Parkinsonism-Dystonia, infantile, NGS genetic testing can be used to identify mutations or variations in the SLC6A3 gene that may be responsible for the condition. By analyzing the patient’s DNA, NGS genetic testing can provide information about specific genetic changes that may be causing or contributing to Parkinsonism-Dystonia, infantile. This information can help with diagnosis, prognosis, and potentially guide treatment decisions.

It is important to note that NGS genetic testing is typically performed by a medical geneticist or genetic counselor, and the results should be interpreted by a qualified healthcare professional who specializes in genetics. The test may involve taking a blood or saliva sample from the patient, which is then sent to a laboratory for analysis.

Overall, NGS genetic testing for the SLC6A3 gene can provide valuable insights into the genetic basis of Parkinsonism-Dystonia, infantile and help guide patient management and treatment options.

Test Name	SLC6A3 Gene Parkinsonism-Dystonia infantile 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 SLC6A3 Gene Parkinsonism-Dystonia, infantile NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with SLC6A3 Gene Parkinsonism-Dystonia, infantile
Test Details	The SLC6A3 gene is associated with a condition called Parkinsonism-Dystonia, infantile. This is a genetic disorder characterized by the combination of parkinsonism (movement problems similar to Parkinson’s disease) and dystonia (involuntary muscle contractions). NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses high-throughput sequencing technologies to analyze multiple genes simultaneously. In the context of Parkinsonism-Dystonia, infantile, NGS genetic testing can be used to identify mutations or variations in the SLC6A3 gene that may be responsible for the condition. By analyzing the patient’s DNA, NGS genetic testing can provide information about specific genetic changes that may be causing or contributing to Parkinsonism-Dystonia, infantile. This information can help with diagnosis, prognosis, and potentially guide treatment decisions. It is important to note that NGS genetic testing is typically performed by a medical geneticist or genetic counselor, and the results should be interpreted by a qualified healthcare professional who specializes in genetics. The test may involve taking a blood or saliva sample from the patient, which is then sent to a laboratory for analysis. Overall, NGS genetic testing for the SLC6A3 gene can provide valuable insights into the genetic basis of Parkinsonism-Dystonia, infantile and help guide patient management and treatment options.