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FAM126A Gene Leukodystrophy hypomyelinating type 5 Genetic Test

4,400 د.إ

-21%

The FAM126A gene leukodystrophy, hypomyelinating type 5, is a rare genetic disorder characterized by the abnormal development of white matter in the brain, leading to a range of neurological symptoms such as motor dysfunction, muscle stiffness, and developmental delays. The condition is caused by mutations in the FAM126A gene, which plays a crucial role in the formation and maintenance of myelin, the protective sheath surrounding nerve fibers.

To diagnose this condition, a genetic test can be conducted to identify mutations in the FAM126A gene. DNA Labs UAE offers a specialized genetic testing service for this purpose. The test is designed to provide a definitive diagnosis by analyzing the patient’s DNA for specific mutations associated with hypomyelinating leukodystrophy type 5. This can be particularly useful for confirming the diagnosis in patients exhibiting symptoms of the disorder, as well as for carrier testing in family members of affected individuals.

The cost of the FAM126A gene leukodystrophy hypomyelinating type 5 genetic test at DNA Labs UAE is 4400 AED. This investment covers the comprehensive analysis required to detect the presence of FAM126A gene mutations. Upon completion, the results can offer valuable insights into the patient’s condition, guiding treatment decisions and management strategies to improve quality of life.

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FAM126A Gene Leukodystrophy hypomyelinating type 5 Genetic Test

At DNA Labs UAE, we offer the FAM126A Gene Leukodystrophy hypomyelinating type 5 Genetic Test for individuals who may be at risk for this rare genetic disorder. Leukodystrophies are a group of disorders that affect the white matter of the brain, leading to abnormal myelin formation or maintenance.

Test Components and Price

The FAM126A Gene Leukodystrophy hypomyelinating type 5 Genetic Test is priced at 4400.0 AED. The test can be performed on a blood sample, extracted DNA, or even one drop of blood on an FTA card.

Report Delivery and Method

After the sample is collected, the report will be delivered within 3 to 4 weeks. The test utilizes NGS (Next-Generation Sequencing) technology, which allows for the simultaneous analysis of multiple genes or the entire genome.

Test Type and Doctor

The FAM126A Gene Leukodystrophy hypomyelinating type 5 Genetic Test falls under the category of Neurological Disorders. It is recommended to consult with a Neurologist for this specific test.

Test Department and Pre Test Information

The test is conducted in our Genetics department. Before undergoing the FAM126A Gene Leukodystrophy hypomyelinating type 5 NGS Genetic DNA Test, it is essential to provide the clinical history of the patient. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected by this specific genetic disorder.

About FAM126A Gene Leukodystrophy hypomyelinating type 5

The FAM126A gene is associated with a type of leukodystrophy called hypomyelinating type 5. This genetic disorder affects the white matter of the brain, leading to abnormal myelin formation or maintenance. By analyzing the DNA sequence of the FAM126A gene, NGS genetic testing can help identify specific mutations or variants that may be causing hypomyelinating type 5 leukodystrophy.

It is important to note that genetic testing for leukodystrophies, including hypomyelinating type 5, should be conducted and interpreted by healthcare professionals with expertise in genetics and neurology. They can provide more detailed information about the specific genetic test, its accuracy, and its implications for an individual or family.

Test Name FAM126A Gene Leukodystrophy hypomyelinating type 5 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 FAM126A Gene Leukodystrophy hypomyelinating type 5 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with FAM126A Gene Leukodystrophy hypomyelinating type 5
Test Details

The FAM126A gene is associated with a type of leukodystrophy called hypomyelinating type 5. Leukodystrophies are a group of rare genetic disorders that affect the white matter of the brain, leading to abnormal myelin formation or maintenance.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that allows for the simultaneous analysis of multiple genes or the entire genome. In the context of leukodystrophies, NGS can be used to identify mutations or variants in genes associated with these disorders, including the FAM126A gene.

By analyzing the DNA sequence of the FAM126A gene, NGS genetic testing can help identify specific mutations or variants that may be causing hypomyelinating type 5 leukodystrophy. This information can be useful for confirming a diagnosis, understanding disease progression, and potentially guiding treatment options or genetic counseling.

It’s important to note that genetic testing for leukodystrophies, including hypomyelinating type 5, should be conducted and interpreted by healthcare professionals with expertise in genetics and neurology. They can provide more detailed information about the specific genetic test, its accuracy, and its implications for an individual or family.