At DNA Labs UAE, we are committed to providing our clients with comprehensive genetic testing services to identify a range of genetic conditions, including the CXCR4 Gene WHIM Syndrome. WHIM syndrome is a rare genetic disorder characterized by warts, hypogammaglobulinemia, infections, and myelokathexis. This article aims to provide detailed information on the symptoms of CXCR4 Gene WHIM Syndrome and the genetic testing available for this condition at DNA Labs UAE.
Symptoms of CXCR4 Gene WHIM Syndrome
WHIM Syndrome, associated with mutations in the CXCR4 gene, manifests through a variety of symptoms that can affect an individual’s quality of life. Recognizing these symptoms early on is crucial for the management and treatment of the condition. The primary symptoms of WHIM Syndrome include:
- Warts: Individuals with WHIM Syndrome often develop warts on the skin or mucous membranes. These warts can be extensive and difficult to treat.
- Hypogammaglobulinemia: This condition involves a decrease in all types of gamma globulins, including antibodies that help fight infections. As a result, individuals with WHIM Syndrome are more susceptible to infections.
- Infections: People with WHIM Syndrome experience recurrent bacterial infections due to the immune system’s inability to produce a sufficient amount of antibodies. These infections can be more severe and occur more frequently than in the general population.
- Myelokathexis: This is a condition where neutrophils (a type of white blood cell) are retained in the bone marrow and not released into the bloodstream, leading to a low count of neutrophils (neutropenia). This further increases the risk of infections.
Other symptoms may include anemia, leukopenia (a reduction in the number of white cells in the blood), and lymphopenia (a condition of having an abnormally low level of lymphocytes in the blood). Individuals with WHIM Syndrome may also experience bone marrow abnormalities and an increased risk of developing certain types of cancer.
CXCR4 Gene WHIM Syndrome Genetic Test at DNA Labs UAE
At DNA Labs UAE, we offer a genetic test for the CXCR4 Gene WHIM Syndrome to help diagnose this condition accurately. This test is crucial for individuals experiencing the symptoms mentioned above or those with a family history of WHIM Syndrome. Early diagnosis can significantly impact the management and treatment options for individuals with this condition.
The test involves a simple blood draw and is priced at 4400 AED. Our state-of-the-art laboratory is equipped with the latest technology to ensure accurate and reliable results. Our team of genetic counselors and medical professionals is available to guide you through the testing process and help interpret the results.
For more information about the CXCR4 Gene WHIM Syndrome Genetic Test and to schedule your test, please visit our website at DNA Labs UAE.
Understanding the symptoms and undergoing genetic testing for WHIM Syndrome is a step forward in managing this condition effectively. At DNA Labs UAE, we are here to support you throughout this journey with our comprehensive testing services and expert guidance.
