ARX Gene Partington Syndrome Genetic Test
At DNA Labs UAE, we offer the ARX Gene Partington Syndrome Genetic Test to help individuals diagnose and understand this rare genetic disorder. This test analyzes the ARX gene for mutations or abnormalities associated with Partington syndrome, a condition characterized by intellectual disability, seizures, and other neurological abnormalities.
Test Components and Price
The ARX Gene Partington Syndrome Genetic Test costs AED 4400.0. The test can be conducted using a blood sample, extracted DNA, or one drop of blood on an FTA card.
Report Delivery
After the test is conducted, the report will be delivered within 3 to 4 weeks.
Method and Test Type
The ARX Gene Partington Syndrome Genetic Test utilizes NGS (Next-Generation Sequencing) technology. This allows for the simultaneous analysis of multiple genes, including the ARX gene, in a single test. The test falls under the category of neurological disorders.
Doctor and Test Department
The test is performed by a neurologist and falls under the genetics department.
Pre Test Information
Prior to conducting the ARX Gene Partington Syndrome Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session is recommended to draw a pedigree chart of family members affected by ARX Gene Partington syndrome.
Test Details
The ARX Gene Partington Syndrome Genetic Test is designed to identify mutations or abnormalities in the ARX gene associated with Partington syndrome. The test helps confirm a diagnosis, provide information about the genetic cause of the syndrome, and aid in genetic counseling and family planning decisions.
This test utilizes NGS technology, which allows for the analysis of various types of mutations, including point mutations, insertions, deletions, and rearrangements. It is typically recommended for individuals with symptoms suggestive of Partington syndrome or a family history of the condition.
The test is performed on a blood or saliva sample, and the DNA is extracted and sequenced using NGS technology. Geneticists and bioinformaticians analyze the obtained genetic data to identify any mutations or variants in the ARX gene associated with Partington syndrome.
It is important to note that genetic testing for Partington syndrome is typically ordered by healthcare professionals specializing in genetics or neurology. The test results should be interpreted by a qualified healthcare provider, taking into consideration the individual’s clinical presentation and family history.
Genetic Counseling
Genetic counseling is highly recommended to discuss the implications of the test results and provide guidance on management and family planning options.
| Test Name | ARX Gene Partington syndrome 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 ARX Gene Partington syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with ARX Gene Partington syndrome |
| Test Details |
ARX Gene Partington syndrome NGS Genetic Test is a type of genetic test that analyzes the ARX gene for mutations or abnormalities associated with Partington syndrome. Partington syndrome is a rare genetic disorder characterized by intellectual disability, seizures, and other neurological abnormalities. The ARX gene is responsible for producing a protein that plays a crucial role in brain development. The NGS (Next-Generation Sequencing) technology used in this test allows for the simultaneous analysis of multiple genes, including the ARX gene, in a single test. It can identify various types of mutations, such as point mutations, insertions, deletions, and rearrangements, that may be responsible for causing Partington syndrome. The ARX Gene Partington syndrome NGS Genetic Test is typically recommended for individuals with symptoms suggestive of Partington syndrome or a family history of the condition. It can help confirm a diagnosis, provide information about the genetic cause of the syndrome, and aid in genetic counseling and family planning decisions. The test is usually performed on a blood or saliva sample, and the DNA is extracted and sequenced using NGS technology. The obtained genetic data is then analyzed by geneticists and bioinformaticians to identify any mutations or variants in the ARX gene that may be associated with Partington syndrome. It is important to note that genetic testing for Partington syndrome is typically ordered by healthcare professionals who specialize in genetics or neurology. The test results should be interpreted in conjunction with the individual’s clinical presentation and family history by a qualified healthcare provider. Genetic counseling is also recommended to discuss the implications of the test results and provide guidance on management and family planning options. |
