Sale!

CPT1C Gene SPG73 Genetic Test Cost

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

-21%

The “CPT1C Gene SPG73 Genetic Test” is a specialized diagnostic tool designed to identify mutations in the CPT1C gene, which have been associated with spastic paraplegia 73 (SPG73), a rare neurological disorder characterized by progressive weakness and stiffness of the legs. This genetic testing is crucial for individuals displaying symptoms of SPG73, as it can provide definitive diagnosis, enabling tailored management and treatment plans. Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, the test ensures high accuracy and reliability. The cost of the test is set at 4400 AED, reflecting the sophisticated technology and expertise involved in detecting the specific gene mutations responsible for the condition. This test is a significant step forward in the field of neurogenetics, offering hope and direction for affected individuals and their families.

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

CPT1C Gene SPG73 Genetic Test

At DNA Labs UAE, we offer the CPT1C Gene SPG73 Genetic Test for the diagnosis of hereditary spastic paraplegia (HSP). This neurodegenerative disorder is characterized by progressive stiffness and weakness of the leg muscles, leading to difficulty walking.

Test Details

The CPT1C gene, also known as SPG73, is associated with HSP. To analyze the DNA sequence of an individual’s genes, we use NGS (Next-Generation Sequencing) technology. This method allows us to detect genetic variations, such as mutations or changes, in specific genes, including the CPT1C gene.

Our CPT1C Gene SPG73 NGS genetic test involves sequencing the CPT1C gene in individuals suspected of having HSP. By identifying any disease-causing mutations in the CPT1C gene, this test can help confirm a diagnosis of HSP.

Test Components and Price

Our CPT1C Gene SPG73 Genetic Test is priced at 4400.0 AED. The test can be performed using blood or extracted DNA, or even one drop of blood on an FTA Card.

Report Delivery

The report for the CPT1C Gene SPG73 Genetic Test is typically delivered within 3 to 4 weeks.

Test Type and Department

The CPT1C Gene SPG73 Genetic Test falls under the category of Neurological Disorders. It is conducted in our Genetics department.

Pre-Test Information

Prior to the test, it is essential to provide the clinical history of the patient who is going for the CPT1C Gene SPG73 NGS Genetic DNA Test. Additionally, a Genetic Counselling session is recommended to draw a pedigree chart of family members affected by CPT1C Gene SPG73.

Doctor and Test Department

The CPT1C Gene SPG73 Genetic Test is performed under the supervision of a Neurologist and is conducted in our Genetics department.

Benefits of Genetic Testing

Genetic testing can provide valuable information about the inheritance pattern of HSP, which can be helpful for family planning and genetic counseling purposes. It can also aid in predicting the severity and progression of the disease, allowing for better management and treatment options.

It’s important to note that genetic testing should always be done under the guidance of a healthcare professional or genetic counselor. They can interpret the results and provide appropriate recommendations and support.

Test Name CPT1C Gene SPG73 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 CPT1C Gene SPG73 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with CPT1C Gene SPG73
Test Details

The CPT1C gene, also known as SPG73, is associated with a neurodegenerative disorder called hereditary spastic paraplegia (HSP). HSP is characterized by progressive stiffness and weakness of the leg muscles, leading to difficulty walking.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual’s genes. It allows for the detection of genetic variations, such as mutations or changes, in specific genes, including the CPT1C gene.

A CPT1C gene SPG73 NGS genetic test would involve sequencing the CPT1C gene in an individual suspected of having HSP. This test can help confirm a diagnosis of HSP by identifying any disease-causing mutations in the CPT1C gene.

Genetic testing can also provide information about the inheritance pattern of HSP, which can be helpful for family planning and genetic counseling purposes. Additionally, it can aid in predicting the severity and progression of the disease, allowing for better management and treatment options.

It’s important to note that genetic testing should be done under the guidance of a healthcare professional or genetic counselor, who can interpret the results and provide appropriate recommendations and support.