L1CAM Gene SPG1 Genetic Test sale cost 4400 AED
MYH7 Gene Scapuloperoneal Myopathy MYH7 Related Genetic Test sale cost 4400 AED MYH7 Gene Scapuloperoneal Myopathy MYH7 Related Genetic Test Cost 5,600 د.إ Original price was: 5,600 د.إ.4,400 د.إCurrent price is: 4,400 د.إ.
PNPLA6 Gene SPG39 Genetic Test sale cost 4400 AED PNPLA6 Gene SPG39 Genetic Test Cost 5,600 د.إ Original price was: 5,600 د.إ.4,400 د.إCurrent price is: 4,400 د.إ.
Sale!

L1CAM Gene SPG1 Genetic Test Cost

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

-21%

The L1CAM gene SPG1 genetic test is a specialized diagnostic procedure designed to identify mutations in the L1 cell adhesion molecule (L1CAM) gene, which are known to cause X-linked hydrocephalus and MASA (mental retardation, aphasia, shuffling gait, and adducted thumbs) syndrome, as well as contribute to the development of spastic paraplegia 1 (SPG1). This test is crucial for individuals showing symptoms of these conditions or for families with a history of related genetic disorders, as early diagnosis can lead to better management and understanding of the condition.

Conducted at DNA Labs UAE, a leading facility in genetic testing and analysis, the L1CAM gene SPG1 genetic test is performed with cutting-edge technology to ensure high accuracy and reliability of results. The test involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed for specific mutations in the L1CAM gene that are indicative of the aforementioned conditions.

The cost of the L1CAM gene SPG1 genetic test at DNA Labs UAE is set at 4400 AED. This cost reflects the comprehensive nature of the test, including the sophisticated analysis and the expertise required to interpret the results accurately. Individuals considering this test are advised to consult with a genetic counselor or healthcare provider to understand the implications of the results and the next steps in the management or treatment of the condition.

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

L1CAM Gene SPG1 Genetic Test

At DNA Labs UAE, we offer the L1CAM Gene SPG1 Genetic Test for individuals suspected of having hereditary spastic paraplegia type 1 (SPG1). This diagnostic test utilizes next-generation sequencing (NGS) technology to analyze the L1CAM gene for mutations associated with SPG1.

Test Details

The L1CAM gene SPG1 NGS genetic test is a comprehensive examination that can identify various types of mutations in the L1CAM gene, including single nucleotide variants, small insertions or deletions, and larger structural rearrangements. This test is particularly useful for confirming a diagnosis of SPG1 in individuals exhibiting clinical symptoms of the condition.

Additionally, the L1CAM gene SPG1 NGS genetic test can be utilized for carrier testing in individuals with a family history of SPG1, as well as for prenatal testing in families with a known L1CAM gene mutation. The results of this test provide crucial information for patient management and can also indicate the risk of passing on the condition to offspring.

Components and Price

The L1CAM Gene SPG1 Genetic Test is priced at 4400.0 AED. The test requires a blood sample or extracted DNA, or alternatively, one drop of blood on an FTA card. The report delivery time is estimated to be 3 to 4 weeks.

Method and Test Type

The L1CAM Gene SPG1 Genetic Test utilizes NGS technology, which enables the simultaneous analysis of multiple genes, including the L1CAM gene, in a single test. This advanced method ensures accurate and efficient detection of mutations associated with SPG1.

The test falls under the category of Neurological Disorders and is performed by our specialized Genetics department, with a focus on assisting Neurologists in diagnosing and managing patients with suspected SPG1.

Pre Test Information

Prior to undergoing the L1CAM Gene SPG1 Genetic Test, it is recommended to provide the clinical history of the patient who will be tested. This information helps our team better understand the individual’s symptoms and medical background.

In addition, a Genetic Counselling session is advised to draw a pedigree chart of family members affected by SPG1. This chart assists in assessing the inheritance pattern and identifying potential carriers within the family.

Genetic Counseling and Patient Support

Genetic counseling plays a crucial role in the process of genetic testing. Before and after the L1CAM Gene SPG1 Genetic Test, our experienced genetic counselors are available to discuss the implications of the results and assist individuals in making informed decisions.

We understand that genetic testing can be a complex and emotional journey. Our dedicated team is committed to providing ongoing support and guidance to patients and their families throughout the testing process.

For more information or to schedule an appointment for the L1CAM Gene SPG1 Genetic Test, please contact our Neurology department.

Test Name L1CAM Gene SPG1 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 L1CAM Gene SPG1 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with L1CAM Gene SPG1
Test Details

The L1CAM gene SPG1 NGS genetic test is a diagnostic test that uses next-generation sequencing (NGS) technology to analyze the L1CAM gene for mutations associated with hereditary spastic paraplegia type 1 (SPG1).

Hereditary spastic paraplegia (HSP) is a group of genetic disorders characterized by progressive weakness and stiffness of the legs (paraplegia) due to degeneration of the corticospinal tracts in the spinal cord. SPG1 is one of the most common forms of HSP and is caused by mutations in the L1CAM gene.

NGS technology allows for the simultaneous analysis of multiple genes, including the L1CAM gene, in a single test. This test can identify various types of mutations in the L1CAM gene, such as single nucleotide variants, small insertions or deletions, and larger structural rearrangements.

The L1CAM gene SPG1 NGS genetic test can help confirm a diagnosis of SPG1 in individuals with clinical symptoms suggestive of the condition. It can also be used for carrier testing in individuals with a family history of SPG1 or for prenatal testing in families with a known L1CAM gene mutation.

The results of the test can guide patient management and provide information on the risk of passing on the condition to offspring. Genetic counseling is typically recommended before and after undergoing genetic testing to discuss the implications of the results and to help individuals make informed decisions.

SKU: TEST-1987 Category:

Related products