GALC Gene Krabbe Disease Genetic Test
At DNA Labs UAE, we offer the GALC Gene Krabbe Disease Genetic Test for individuals who suspect they may have Krabbe disease or have a family history of the condition. This test is designed to analyze the GALC gene and identify any genetic variations or mutations that may be present.
Test Components
- Price: 4400.0 AED
- Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery
Results for the GALC Gene Krabbe Disease Genetic Test are typically delivered within 3 to 4 weeks.
Method
The GALC Gene Krabbe Disease Genetic Test utilizes Next-Generation Sequencing (NGS) technology. NGS allows for the sequencing of multiple genes simultaneously, providing a more comprehensive analysis compared to traditional sequencing methods.
Test Type
The GALC Gene Krabbe Disease Genetic Test falls under the category of Neurological Disorders.
Doctor
This test is recommended to be performed under the supervision of a Neurologist.
Test Department
The GALC Gene Krabbe Disease Genetic Test is conducted in our Genetics department.
Pre Test Information
Prior to undergoing the GALC Gene Krabbe Disease Genetic Test, it is important 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 GALC Gene Krabbe disease.
Test Details
The GALC (galactosylceramidase) gene is associated with Krabbe disease, also known as globoid cell leukodystrophy. Krabbe disease is a rare genetic disorder that affects the nervous system, specifically the myelin sheath, which is the protective covering around nerve fibers.
The NGS technology used in this test allows for a more accurate and efficient way of diagnosing genetic disorders. It can detect both common and rare genetic variants, providing a comprehensive analysis of the GALC gene.
The GALC Gene Krabbe Disease Genetic Test can help in confirming a diagnosis, guiding treatment decisions, and providing information about the risk of passing on the condition to future generations. It can also be used for prenatal testing in families with a known GALC gene mutation to determine the risk of Krabbe disease in a fetus.
It is important to consult with a healthcare professional or genetic counselor to discuss the appropriateness and availability of NGS testing for Krabbe disease and to understand the implications of the test results.
Test Name | GALC Gene Krabbe 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 GALC Gene Krabbe disease NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with GALC Gene Krabbe disease |
Test Details |
GALC (galactosylceramidase) gene is associated with Krabbe disease, also known as globoid cell leukodystrophy. Krabbe disease is a rare genetic disorder that affects the nervous system, specifically the myelin sheath, which is the protective covering around nerve fibers. NGS (Next-Generation Sequencing) is a type of genetic testing that can be used to analyze the GALC gene and identify any genetic variations or mutations that may be present. This test can help in the diagnosis of Krabbe disease and can also be used for carrier screening in individuals with a family history of the condition. NGS technology allows for the sequencing of multiple genes simultaneously, providing a more comprehensive analysis compared to traditional sequencing methods. It can detect both common and rare genetic variants, offering a more accurate and efficient way of diagnosing genetic disorders. In the context of Krabbe disease, an NGS genetic test for GALC gene can help in confirming a diagnosis, guiding treatment decisions, and providing information about the risk of passing on the condition to future generations. It can also be used for prenatal testing in families with a known GALC gene mutation to determine the risk of Krabbe disease in a fetus. It is important to consult with a healthcare professional or a genetic counselor to discuss the appropriateness and availability of NGS testing for Krabbe disease and to understand the implications of the test results. |