PSEN1 Gene Pick Disease Genetic Test
Test Name: PSEN1 Gene Pick Disease Genetic Test
Components: Blood or Extracted DNA or One drop Blood on FTA Card
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 PSEN1 Gene Pick Disease NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PSEN1 Gene Pick Disease.
Test Details
The PSEN1 gene is associated with Pick disease, which is a rare neurodegenerative disorder characterized by progressive cognitive decline, behavioral changes, and language impairment. Next-generation sequencing (NGS) genetic testing can be used to analyze the PSEN1 gene for any mutations or variations that may be responsible for the development of Pick disease.
NGS technology allows for the simultaneous sequencing of multiple genes, including the PSEN1 gene, in a more efficient and cost-effective manner compared to traditional sequencing methods. By analyzing the entire coding region of the PSEN1 gene, NGS testing can identify any pathogenic mutations or variations that may be present.
The NGS genetic test for PSEN1 gene mutations can be used for diagnostic purposes in individuals suspected to have Pick disease based on their clinical symptoms and family history. It can also be used for carrier testing in individuals with a family history of Pick disease who may be at risk of passing on the genetic mutation to their children.
Identifying PSEN1 gene mutations through NGS testing can help in confirming the diagnosis of Pick disease, providing information about disease progression and prognosis, and guiding treatment decisions. It can also be useful for genetic counseling and family planning purposes.
It is important to note that genetic testing should be conducted and interpreted by qualified healthcare professionals with expertise in genetic counseling and neurogenetics. The results of genetic testing should be interpreted in conjunction with clinical findings and family history to provide an accurate diagnosis and appropriate management plan for individuals suspected to have Pick disease.
| Test Name | PSEN1 Gene Pick disease 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 PSEN1 Gene Pick disease NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with PSEN1 Gene Pick disease |
| Test Details |
PSEN1 gene is associated with Pick disease, which is a rare neurodegenerative disorder characterized by progressive cognitive decline, behavioral changes, and language impairment. Next-generation sequencing (NGS) genetic testing can be used to analyze the PSEN1 gene for any mutations or variations that may be responsible for the development of Pick disease. NGS technology allows for the simultaneous sequencing of multiple genes, including the PSEN1 gene, in a more efficient and cost-effective manner compared to traditional sequencing methods. By analyzing the entire coding region of the PSEN1 gene, NGS testing can identify any pathogenic mutations or variations that may be present. The NGS genetic test for PSEN1 gene mutations can be used for diagnostic purposes in individuals suspected to have Pick disease based on their clinical symptoms and family history. It can also be used for carrier testing in individuals with a family history of Pick disease who may be at risk of passing on the genetic mutation to their children. Identifying PSEN1 gene mutations through NGS testing can help in confirming the diagnosis of Pick disease, providing information about disease progression and prognosis, and guiding treatment decisions. It can also be useful for genetic counseling and family planning purposes. It is important to note that genetic testing should be conducted and interpreted by qualified healthcare professionals with expertise in genetic counseling and neurogenetics. The results of genetic testing should be interpreted in conjunction with clinical findings and family history to provide an accurate diagnosis and appropriate management plan for individuals suspected to have Pick disease. |
