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HSPD1 Gene Leukodystrophy hypomyelinating type 4 Genetic Test

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

-21%

The HSPD1 Gene Leukodystrophy Hypomyelinating Type 4 Genetic Test is a specialized diagnostic tool designed to identify mutations in the HSPD1 gene, which are associated with Hypomyelinating Leukodystrophy Type 4. This condition is a rare genetic disorder characterized by the insufficient formation of myelin, the protective sheath around nerve cells in the brain, leading to neurological problems. The test is crucial for confirming the diagnosis, understanding the disease progression, and guiding treatment decisions.

Performed at DNA Labs UAE, a leading facility in genetic testing, the test involves analyzing the patient’s DNA to look for specific mutations in the HSPD1 gene that are known to cause the disorder. The process is meticulous and requires a sample of the patient’s blood or saliva.

The cost of the test is set at 4400 AED, reflecting the comprehensive analysis and the specialized technology employed to detect the mutations accurately. Getting tested at DNA Labs UAE ensures that patients and their families receive reliable results, thanks to the lab’s commitment to high standards of testing and its use of cutting-edge genetic technologies. This test is an essential step for families seeking answers to complex genetic disorders, offering them a path towards better management and understanding of Hypomyelinating Leukodystrophy Type 4.

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  • This test is not intended for medical diagnosis or treatment
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HSPD1 Gene Leukodystrophy hypomyelinating type 4 Genetic Test

Welcome to DNA Labs UAE, where we offer the HSPD1 Gene Leukodystrophy hypomyelinating type 4 Genetic Test. This test is designed to analyze the HSPD1 gene and identify any mutations or variations that may be present in individuals with leukodystrophy hypomyelinating type 4.

Test Components

  • 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

Before undergoing the HSPD1 Gene Leukodystrophy hypomyelinating type 4 Genetic Test, it is important to provide a clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected with HSPD1 Gene Leukodystrophy hypomyelinating type 4.

Test Details

The HSPD1 gene is associated with a rare genetic disorder called leukodystrophy hypomyelinating type 4. This disorder affects the development and maintenance of myelin, the protective covering of nerve fibers in the brain and spinal cord. Mutations in the HSPD1 gene can disrupt the function of a protein called heat shock protein 60 (HSP60), which is involved in the proper folding of other proteins.

A next-generation sequencing (NGS) genetic test can be used to analyze the HSPD1 gene and identify any mutations or variations that may be present. This type of test can provide valuable information about the genetic cause of leukodystrophy hypomyelinating type 4 and help in making a diagnosis.

NGS genetic testing involves sequencing the DNA of an individual to identify specific variations or mutations in genes of interest. This can be done using a small blood sample or other tissue samples. The DNA sequence data is then compared to a reference sequence to identify any differences.

Genetic testing for leukodystrophy hypomyelinating type 4 can be helpful for confirming a diagnosis, predicting the likelihood of passing the condition on to offspring, and providing information for genetic counseling. It may also be used for research purposes to better understand the disease and develop potential treatments.

Test Name HSPD1 Gene Leukodystrophy hypomyelinating type 4 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 HSPD1 Gene Leukodystrophy hypomyelinating type 4 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with HSPD1 Gene Leukodystrophy hypomyelinating type 4
Test Details

The HSPD1 gene is associated with a rare genetic disorder called leukodystrophy hypomyelinating type 4. This disorder affects the development and maintenance of myelin, the protective covering of nerve fibers in the brain and spinal cord. Mutations in the HSPD1 gene can disrupt the function of a protein called heat shock protein 60 (HSP60), which is involved in the proper folding of other proteins.

A next-generation sequencing (NGS) genetic test can be used to analyze the HSPD1 gene and identify any mutations or variations that may be present. This type of test can provide valuable information about the genetic cause of leukodystrophy hypomyelinating type 4 and help in making a diagnosis.

NGS genetic testing involves sequencing the DNA of an individual to identify specific variations or mutations in genes of interest. This can be done using a small blood sample or other tissue samples. The DNA sequence data is then compared to a reference sequence to identify any differences.

Genetic testing for leukodystrophy hypomyelinating type 4 can be helpful for confirming a diagnosis, predicting the likelihood of passing the condition on to offspring, and providing information for genetic counseling. It may also be used for research purposes to better understand the disease and develop potential treatments.