Sale!

SPG7 Gene SPG7 Genetic Test Cost

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

-21%

The SPG7 gene is associated with a condition known as spastic paraplegia 7 (SPG7), a form of hereditary spastic paraplegia. This genetic disorder is characterized by progressive weakness and stiffness of the legs, resulting from the degeneration of nerve pathways responsible for muscle movement and sensation. The SPG7 gene encodes a protein called paraplegin, which is involved in the maintenance and function of mitochondria, the energy-producing structures within cells. Mutations in the SPG7 gene disrupt the normal function of paraplegin, leading to the symptoms associated with the condition.

To diagnose this genetic condition, an SPG7 genetic test is conducted. This test specifically looks for mutations in the SPG7 gene that are known to cause spastic paraplegia 7. It is a crucial step in confirming the diagnosis, understanding the inheritance pattern, and guiding management and treatment decisions for affected individuals and their families.

In the UAE, DNA Labs UAE offers the SPG7 genetic test. The cost of the test is 4400 AED. DNA Labs UAE is equipped with advanced genetic testing technology to ensure accurate and reliable results. By opting for this test, patients and their healthcare providers can gain valuable insights into the genetic basis of their condition, enabling a more tailored approach to treatment and management.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
Guaranteed Safe Checkout

SPG7 Gene SPG7 Genetic Test

Test Name: SPG7 Gene SPG7 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 SPG7 Gene SPG7 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SPG7 Gene SPG7.

Test Details

The SPG7 gene is responsible for producing the protein paraplegin, which is involved in the maintenance and function of mitochondria. Mutations in the SPG7 gene can lead to a condition called hereditary spastic paraplegia type 7 (HSP7), which is characterized by progressive muscle weakness and stiffness in the legs.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. In the case of SPG7 gene testing, NGS can be used to identify any mutations or variations in the SPG7 gene that may be causing or predisposing an individual to hereditary spastic paraplegia type 7.

NGS genetic testing for SPG7 can help in the diagnosis of HSP7, as well as provide information about the specific mutation(s) present in the SPG7 gene. This information can be useful for genetic counseling, as well as for understanding the underlying cause of the condition and potentially guiding treatment decisions.

It is important to note that genetic testing for SPG7 and other genetic conditions should be performed and interpreted by a qualified healthcare professional or genetic counselor, as they can provide guidance and support throughout the testing process and help interpret the results accurately.

Test Name SPG7 Gene SPG7 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 SPG7 Gene SPG7 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with SPG7 Gene SPG7
Test Details

The SPG7 gene is responsible for producing the protein paraplegin, which is involved in the maintenance and function of mitochondria. Mutations in the SPG7 gene can lead to a condition called hereditary spastic paraplegia type 7 (HSP7), which is characterized by progressive muscle weakness and stiffness in the legs.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. In the case of SPG7 gene testing, NGS can be used to identify any mutations or variations in the SPG7 gene that may be causing or predisposing an individual to hereditary spastic paraplegia type 7.

NGS genetic testing for SPG7 can help in the diagnosis of HSP7, as well as provide information about the specific mutation(s) present in the SPG7 gene. This information can be useful for genetic counseling, as well as for understanding the underlying cause of the condition and potentially guiding treatment decisions.

It is important to note that genetic testing for SPG7 and other genetic conditions should be performed and interpreted by a qualified healthcare professional or genetic counselor, as they can provide guidance and support throughout the testing process and help interpret the results accurately.