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PLP1 Gene Pelizaeus-Merzbacher Disease Genetic Test Cost

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

-21%

The PLP1 gene Pelizaeus-Merzbacher Disease (PMD) genetic test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the PLP1 gene, which are responsible for causing Pelizaeus-Merzbacher Disease. PMD is a rare, genetic, central nervous system disorder characterized by a range of neurological symptoms, including motor abilities impairment, cognitive development issues, and coordination problems. The test is crucial for early diagnosis, which can aid in managing symptoms and improving the quality of life for affected individuals. The cost of the test is 4400 AED, making it an accessible option for those seeking comprehensive genetic analysis in the UAE. This test is particularly valuable for families with a history of PMD, offering them crucial information for family planning and management of the condition.

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PLP1 Gene Pelizaeus-Merzbacher disease Genetic Test

At DNA Labs UAE, we offer the PLP1 Gene Pelizaeus-Merzbacher disease Genetic Test to diagnose this rare genetic disorder affecting the central nervous system. This test can help identify mutations or variations in the PLP1 gene responsible for Pelizaeus-Merzbacher disease (PMD).

Test Details

Pelizaeus-Merzbacher disease (PMD) is characterized by abnormal myelin formation in the brain, leading to neurological symptoms such as impaired motor skills, muscle weakness, and cognitive impairment. Our Next-generation sequencing (NGS) technology allows for the simultaneous analysis of multiple genes, including the PLP1 gene associated with PMD.

Test Components and Price

  • Test Name: PLP1 Gene Pelizaeus-Merzbacher disease Genetic Test
  • Components: NGS Technology
  • Price: 4400.0 AED

Sample Condition

We accept blood samples, extracted DNA, or one drop of blood on FTA Card for this test.

Report Delivery

You can expect to receive your test results within 3 to 4 weeks.

Test Type and Department

This test falls under the category of Neurological Disorders and is conducted by our Genetics department.

Referring Doctor

This test is recommended by Neurologists who specialize in neurological disorders.

Pre Test Information

Prior to the PLP1 Gene Pelizaeus-Merzbacher disease Genetic Test, we recommend providing the clinical history of the patient. Additionally, a Genetic Counselling session is conducted to draw a pedigree chart of family members affected by PMD.

Why Choose NGS Genetic Testing for PMD?

Next-generation sequencing (NGS) technology allows for a comprehensive analysis of the PLP1 gene, which can provide valuable information for diagnosing PMD and determining the specific genetic cause of the disease. This information is crucial for genetic counseling, family planning, and guiding potential treatment options.

Important Note

It is essential to have the PLP1 Gene Pelizaeus-Merzbacher disease Genetic Test performed by a qualified healthcare professional or genetic counselor. They can interpret the results accurately and provide appropriate guidance and support.

Test Name PLP1 Gene Pelizaeus-Merzbacher 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 PLP1 Gene Pelizaeus-Merzbacher disease NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with PLP1 Gene Pelizaeus-Merzbacher disease
Test Details

The PLP1 gene is associated with Pelizaeus-Merzbacher disease (PMD), which is a rare genetic disorder that affects the central nervous system. PMD is characterized by abnormal myelin formation in the brain, leading to neurological symptoms such as impaired motor skills, muscle weakness, and cognitive impairment.

Next-generation sequencing (NGS) is a genetic testing technique that allows for the simultaneous analysis of multiple genes, including the PLP1 gene. NGS can detect mutations or variations in the PLP1 gene that may be responsible for PMD.

NGS-based genetic testing for PMD involves obtaining a DNA sample, typically through a blood or saliva sample, from the individual being tested. The DNA is then sequenced using NGS technology to identify any mutations or variations in the PLP1 gene.

The results of the NGS genetic test can provide valuable information for diagnosing PMD and determining the specific genetic cause of the disease. This information can be used for genetic counseling, family planning, and potentially guiding treatment options.

It is important to note that genetic testing for PMD should be performed by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate guidance and support.