XK Gene McLeod Syndrome with or without Chronic Granulomatous Disease Genetic Test
At DNA Labs UAE, we offer a comprehensive genetic test for XK Gene McLeod syndrome with or without chronic granulomatous disease. This test is designed to diagnose and provide valuable information about this rare genetic disorder that primarily affects the nervous system and blood cells.
Test Details
XK Gene McLeod syndrome, also known as McLeod neuroacanthocytosis syndrome, is a rare genetic disorder that primarily affects the nervous system and blood cells. It is caused by mutations in the XK gene, which is responsible for producing a protein involved in the movement of certain molecules within red blood cells.
Chronic granulomatous disease (CGD) is another rare genetic disorder that affects the immune system. It is caused by mutations in genes responsible for producing proteins involved in the function of white blood cells, specifically neutrophils. CGD leads to recurrent and severe bacterial and fungal infections due to the impaired ability of neutrophils to kill certain types of pathogens.
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 XK Gene McLeod syndrome with or without chronic granulomatous 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 XK Gene McLeod syndrome with or without chronic granulomatous disease. This information will help in the accurate interpretation of the test results.
NGS Technology
NGS (Next-Generation Sequencing) genetic testing is a high-throughput sequencing technology that allows for the analysis of multiple genes simultaneously. In the case of XK Gene McLeod syndrome with or without chronic granulomatous disease, NGS can be used to identify mutations in the XK gene associated with the syndrome, as well as mutations in genes associated with CGD if relevant. By analyzing the genetic information, NGS can help confirm a diagnosis of XK Gene McLeod syndrome and/or CGD in individuals with suspected symptoms.
Benefits of Genetic Testing
Genetic testing using NGS technology not only helps in confirming the diagnosis of XK Gene McLeod syndrome and/or CGD but also provides valuable information for genetic counseling and potential treatment options. It can be used for carrier testing, prenatal testing, and family planning purposes. The information obtained from the test can guide healthcare professionals in developing personalized treatment plans for affected individuals.
At DNA Labs UAE, we strive to provide accurate and reliable genetic testing services. Our team of experts, including neurologists and geneticists, ensure that every test is performed with utmost precision and care. If you suspect XK Gene McLeod syndrome with or without chronic granulomatous disease, contact us today to schedule a consultation and get started with the genetic testing process.
| Test Name | XK Gene McLeod syndrome with or without chronic granulomatous 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 XK Gene McLeod syndrome with or without chronic granulomatous disease NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with XK Gene McLeod syndrome with or without chronic granulomatous disease |
| Test Details | XK Gene McLeod syndrome, also known as McLeod neuroacanthocytosis syndrome, is a rare genetic disorder that primarily affects the nervous system and blood cells. It is caused by mutations in the XK gene, which is responsible for producing a protein involved in the movement of certain molecules within red blood cells. Chronic granulomatous disease (CGD) is another rare genetic disorder that affects the immune system. It is caused by mutations in genes responsible for producing proteins involved in the function of white blood cells, specifically neutrophils. CGD leads to recurrent and severe bacterial and fungal infections due to the impaired ability of neutrophils to kill certain types of pathogens. NGS (Next-Generation Sequencing) genetic testing is a high-throughput sequencing technology that can be used to analyze multiple genes simultaneously. In the case of XK Gene McLeod syndrome with or without CGD, NGS can be used to identify mutations in the XK gene associated with the syndrome, as well as mutations in genes associated with CGD if relevant. By analyzing the genetic information, NGS can help confirm a diagnosis of XK Gene McLeod syndrome and/or CGD in individuals with suspected symptoms. It can also be used for carrier testing, prenatal testing, and family planning purposes. Additionally, NGS can provide valuable information for genetic counseling and potential treatment options for affected individuals. |
