FLRT1 Gene SPG68 FLRT1 related Genetic Test
Test Name: FLRT1 Gene SPG68 FLRT1 related 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 FLRT1 Gene SPG68, FLRT1 related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FLRT1 Gene SPG68, FLRT1 related.
Test Details
The FLRT1 gene, also known as SPG68, is a gene associated with a neurodevelopmental disorder called hereditary spastic paraplegia type 68 (SPG68). This disorder is characterized by progressive stiffness and weakness in the legs, leading to difficulty walking.
NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes or even the entire genome. In the context of FLRT1 gene testing, NGS can be used to identify mutations or variations in the FLRT1 gene that may be associated with SPG68.
NGS genetic testing for FLRT1-related disorders can help with the diagnosis of SPG68, provide information about the prognosis of the disease, and assist in genetic counseling for affected individuals and their families. It can also aid in the development of targeted therapies and personalized treatment approaches.
It is important to note that genetic testing should be conducted and interpreted by qualified healthcare professionals, such as geneticists or genetic counselors, who can provide appropriate guidance and support.
Test Name | FLRT1 Gene SPG68 FLRT1 related 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 FLRT1 Gene SPG68, FLRT1 related NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with FLRT1 Gene SPG68, FLRT1 related |
Test Details |
The FLRT1 gene, also known as SPG68, is a gene associated with a neurodevelopmental disorder called hereditary spastic paraplegia type 68 (SPG68). This disorder is characterized by progressive stiffness and weakness in the legs, leading to difficulty walking. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes or even the entire genome. In the context of FLRT1 gene testing, NGS can be used to identify mutations or variations in the FLRT1 gene that may be associated with SPG68. NGS genetic testing for FLRT1-related disorders can help with the diagnosis of SPG68, provide information about the prognosis of the disease, and assist in genetic counseling for affected individuals and their families. It can also aid in the development of targeted therapies and personalized treatment approaches. It is important to note that genetic testing should be conducted and interpreted by qualified healthcare professionals, such as geneticists or genetic counselors, who can provide appropriate guidance and support. |