LIPA Gene Wolman Disease Genetic Test
At DNA Labs UAE, we offer the LIPA Gene Wolman Disease Genetic Test for individuals who suspect they may have Wolman disease or have a family history of the condition. This test focuses on analyzing the LIPA gene for mutations associated with Wolman disease, a rare and severe genetic disorder characterized by the buildup of lipids in various organs of the body.
Test Components
- Test Name: LIPA Gene Wolman Disease Genetic Test
- 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: Metabolic Disorders
- Doctor: General Physician
- Test Department: Genetics
Pre Test Information
Prior to undergoing the LIPA Gene Wolman Disease Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected with Wolman disease. This information will assist in the accurate interpretation of the test results.
Test Details
The LIPA Gene Wolman Disease Genetic Test utilizes NGS (Next-Generation Sequencing) technology to analyze the LIPA gene for mutations associated with Wolman disease. The LIPA gene is responsible for producing an enzyme called lysosomal acid lipase (LAL), which is involved in breaking down lipids within cells. Mutations in the LIPA gene can result in reduced or absent LAL activity, leading to the accumulation of lipids and the development of Wolman disease.
During the test, a DNA sample is obtained from the individual being tested. This can be done through a blood or saliva sample. The DNA is then sequenced using NGS technology to identify any mutations or variants in the LIPA gene. The results of the test can help diagnose Wolman disease and provide information about the specific genetic changes contributing to the condition.
The LIPA Gene Wolman Disease Genetic Test is particularly beneficial for individuals with symptoms suggestive of Wolman disease, those with a family history of the condition, or individuals who are carriers of LIPA gene mutations and are planning to have children. Early diagnosis through this genetic test can enable genetic counseling and appropriate management of the disease.
It is important to note that the LIPA Gene Wolman Disease Genetic Test should be ordered and interpreted by a qualified healthcare professional, such as a geneticist or genetic counselor, who can provide proper counseling and guidance based on the test results.
For more information or to schedule a LIPA Gene Wolman Disease Genetic Test, please contact DNA Labs UAE.
| Test Name | LIPA Gene Wolman disease Genetic 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 | Metabolic Disorders |
| Doctor | General Physician |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for LIPA Gene Wolman disease NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Wolman disease |
| Test Details |
LIPA gene Wolman disease NGS genetic test is a type of genetic test that focuses on analyzing the LIPA gene for mutations associated with Wolman disease. Wolman disease is a rare and severe genetic disorder characterized by the buildup of lipids (fats) in various organs of the body, particularly the liver, spleen, and adrenal glands. This buildup of lipids leads to organ dysfunction and can be life-threatening. The LIPA gene is responsible for producing an enzyme called lysosomal acid lipase (LAL), which is involved in breaking down lipids within cells. Mutations in the LIPA gene can result in reduced or absent LAL activity, leading to the accumulation of lipids and the development of Wolman disease. NGS (Next-Generation Sequencing) is a high-throughput DNA sequencing technology that allows for the simultaneous analysis of multiple genes, including the LIPA gene. This technique enables the identification of specific mutations or variants within the LIPA gene that are associated with Wolman disease. The LIPA gene Wolman disease NGS genetic test 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 variants in the LIPA gene. The results of the test can help diagnose Wolman disease and provide information about the specific genetic changes that are contributing to the condition. This genetic test can be useful for individuals with symptoms suggestive of Wolman disease, individuals with a family history of the condition, or individuals who are carriers of LIPA gene mutations and are planning to have children. It can help with early diagnosis, genetic counseling, and management of the disease. It is important to note that this genetic test should be ordered and interpreted by a qualified healthcare professional, such as a geneticist or genetic counselor, who can provide appropriate counseling and guidance based on the test results. |
