The WT-1 Mutation Detection Test is a specialized genetic test designed to identify mutations in the WT1 gene, which plays a crucial role in kidney development and function. Abnormalities in this gene are associated with a range of health issues, most notably Wilms tumor, a type of kidney cancer primarily affecting children, as well as certain syndromes and kidney-related disorders. This test is critical for early diagnosis and guiding treatment strategies, including surgical interventions, chemotherapy, and targeted therapies.
Conducted at DNA Labs UAE, a reputable facility known for its advanced genetic testing services, the test offers a comprehensive analysis of the WT1 gene to detect mutations that could indicate a predisposition to Wilms tumor and other related conditions. The cost of the WT-1 Mutation Detection Test is 2040 AED, reflecting the sophisticated technology and expertise required to accurately identify and interpret genetic variations in the WT1 gene. This investment can be invaluable for affected families, providing essential information for managing and potentially mitigating the impact of associated health issues.
Autoimmune Interstitial Lung Disease (ILD) Panel Test is a diagnostic evaluation aimed at identifying autoimmune disorders that affect the lungs, leading to interstitial lung disease. This condition encompasses a group of diseases causing progressive scarring (fibrosis) of lung tissue, which can significantly impact lung function and overall health. The panel test looks for specific antibodies and markers in the blood that are associated with autoimmune ILDs, helping in the differentiation from other types of lung diseases and guiding appropriate treatment strategies.
The test cost is set at 2120 AED and is conducted at DNA Labs UAE, a leading facility known for its advanced diagnostic services and state-of-the-art laboratory technologies. The lab provides accurate, reliable results, supporting healthcare professionals in making informed decisions regarding patient care. This test is particularly important for individuals presenting symptoms of ILD, such as shortness of breath and chronic cough, as early detection and correct diagnosis can greatly affect the management and prognosis of the disease.
The Collagen Disease Antibodies Panel Test is a comprehensive diagnostic tool designed to detect the presence of specific antibodies in the blood that are associated with various collagen vascular diseases. These diseases are a group of disorders that involve inflammation of the blood vessels and can affect multiple organs and tissues, including the skin, joints, and internal organs. The panel typically includes tests for antibodies such as antinuclear antibodies (ANA), anti-double-stranded DNA (anti-dsDNA), anti-Smith (anti-Sm) antibodies, and others that are indicative of conditions like systemic lupus erythematosus (SLE), rheumatoid arthritis, scleroderma, and mixed connective tissue disease.
At DNA Labs UAE, this comprehensive panel is available for a cost of 2110 AED. The test is conducted with a high degree of accuracy and precision, utilizing advanced laboratory techniques to ensure reliable results. DNA Labs UAE is equipped with state-of-the-art facilities and is staffed by experienced professionals who specialize in the analysis of genetic and autoimmune markers. This test is crucial for individuals experiencing symptoms suggestive of collagen vascular diseases, as it aids in the accurate diagnosis and subsequent management of these conditions. By identifying the specific antibodies present, healthcare providers can tailor treatment plans to address the underlying disease process, improving patient outcomes.
The Cystic Fibrosis Mutation Detection Test is a specialized diagnostic procedure aimed at identifying mutations in the CFTR gene, which are responsible for cystic fibrosis (CF), a genetic disorder that affects the lungs, pancreas, and other organs. This test is crucial for early diagnosis, which can significantly improve the quality of life for individuals with CF by enabling timely and targeted interventions.
Conducted at DNA Labs UAE, a leading facility in genetic testing, the test offers comprehensive screening for the most common mutations associated with cystic fibrosis. Utilizing advanced genetic sequencing technologies, DNA Labs UAE ensures high accuracy and reliability in detecting CFTR gene mutations.
The cost of the Cystic Fibrosis Mutation Detection Test at DNA Labs UAE is 2110 AED. This price reflects the sophisticated nature of the testing process and the invaluable insights it provides for affected individuals and their families. Early detection through this test can lead to better management strategies for cystic fibrosis, ultimately contributing to improved patient outcomes.
The Desmoglein DSG 1 and 3 Antibody in Dilution/End Point Titre Test is a specialized diagnostic procedure designed to detect and measure the levels of antibodies against Desmoglein 1 and Desmoglein 3 in the blood. Desmogleins are critical components of the skin and mucous membranes, playing a pivotal role in cell adhesion, thus maintaining the integrity and function of the epidermis. Autoantibodies against Desmoglein 1 and 3 are hallmarks of autoimmune blistering diseases such as Pemphigus Vulgaris and Pemphigus Foliaceus, respectively. These conditions can lead to severe skin blisters and erosions, impacting patients' quality of life.
The test employs an end point titre methodology, which quantifies the highest dilution of serum at which antibodies can still be detected, providing valuable information on the severity and progression of the disease. This information is crucial for guiding treatment decisions and monitoring response to therapy.
Conducted at DNA Labs UAE, a facility known for its state-of-the-art diagnostic services, the test is priced at 2110 AED. The lab ensures accurate and reliable results, utilizing advanced technologies and methodologies under the supervision of highly qualified professionals. Given the critical nature of diagnosing autoimmune blistering diseases accurately and promptly, the Desmoglein DSG 1 and 3 Antibody in Dilution/End Point Titre Test represents a vital tool in the management of affected patients, aiding in the initiation of appropriate treatments to mitigate symptoms and improve outcomes.
The "Fish - 1p and 19q Codeletion Test" is a specialized diagnostic procedure offered by DNA Labs UAE, designed to detect the deletion of parts of chromosomes 1p and 19q in tumor cells. This test is particularly significant in the context of neuro-oncology, as the presence of 1p and 19q codeletion in oligodendrogliomas, a type of brain tumor, is associated with a better response to chemotherapy and radiotherapy, as well as a longer overall survival. The test employs fluorescence in situ hybridization (FISH), a molecular cytogenetic technique, to identify the chromosomal deletions in tumor samples.
At DNA Labs UAE, the cost for the "Fish - 1p and 19q Codeletion Test" is set at 2110 AED. This price reflects the sophisticated nature of the testing process and the valuable prognostic information it provides, which can significantly influence treatment decisions and outcomes for patients with certain types of brain tumors.
Immunophenotyping by Flow Cytometry Leukemia Diagnostic Panel is a critical test used in the diagnosis and classification of acute leukemia. This advanced diagnostic procedure differentiates between T-cell, B-cell, or Myeloid types of leukemia by analyzing the types of antigens or markers present on the surface of cells. The test involves the use of flow cytometry, a technology that allows for the detailed characterization of individual cells within a sample, making it possible to identify the specific subtype of leukemia a patient has.
Performed at DNA Labs UAE, a leading facility in medical diagnostics, the test offers precise and rapid results, which are crucial for determining the most effective treatment plan for patients. The cost of the test is 2110 AED, an investment in accurate diagnosis and personalized treatment planning. This test is particularly valuable for healthcare professionals and patients alike, providing essential information that guides the therapeutic approach, potentially improving patient outcomes in the battle against leukemia.
Immunophenotyping by Flow Cytometry Leukemia Diagnostic Panel, specifically for CLL (Chronic Lymphocytic Leukemia), HCL (Hairy Cell Leukemia), and SLL (Small Lymphocytic Lymphoma), is a sophisticated diagnostic test available at DNA Labs UAE. Priced at 2110 AED, this test is a critical tool in the diagnosis and classification of these hematologic malignancies. Flow cytometry is a technology that allows for the detailed analysis of the physical and chemical characteristics of cells in a fluid as they pass through a laser beam. This method is instrumental in identifying specific markers on the surface of cells, which are indicative of various types of leukemia.
The CLL/HCL/SLL Basic Test panel is designed to detect the unique immunophenotypic signatures associated with each of these leukemias, enabling precise diagnosis and aiding in the determination of the most effective treatment strategy. By assessing the expression of specific cell surface proteins, this test can distinguish between these closely related diseases, which is crucial for prognosis and management. Conducted at the state-of-the-art facilities of DNA Labs UAE, the test represents an essential step in the journey towards personalized medicine for patients with leukemia, providing them with a targeted approach to treatment based on their specific disease profile.
The Neuronal Paraneoplastic Autoantibodies Profile Test is a specialized diagnostic tool used to detect the presence of specific autoantibodies in the blood that are associated with paraneoplastic syndromes—a group of rare disorders triggered by an immune system response to a cancerous tumor. These autoantibodies target normal components of the nervous system, leading to neurological symptoms that often precede the diagnosis of cancer. Identifying these autoantibodies can be crucial for early cancer detection and the management of neurological symptoms.
Performed at DNA Labs UAE, a leading facility in advanced diagnostic services, this test provides a comprehensive analysis of the autoantibodies related to neuronal paraneoplastic syndromes. The cost of the test is 2110 AED, reflecting the intricate processes involved in detecting these specific autoantibodies. By offering this test, DNA Labs UAE plays a pivotal role in aiding the early diagnosis and treatment planning for patients experiencing neurological symptoms that may be linked to an underlying malignancy, thereby improving patient outcomes.
The Vitamin B6 Pyridoxine Test is a diagnostic procedure conducted to measure the levels of Vitamin B6 in the blood. Vitamin B6, also known as Pyridoxine, is crucial for various bodily functions including metabolism, brain development, and immune system health. Abnormal levels can lead to a range of health issues, from anemia to nerve damage. This test is particularly important for individuals experiencing symptoms of deficiency or toxicity, or those at risk due to dietary restrictions or certain medical conditions.
The test is offered by DNA Labs UAE, a leading provider of diagnostic and genetic testing services in the United Arab Emirates. With state-of-the-art facilities and a commitment to accuracy and reliability, DNA Labs UAE ensures that patients receive precise results to guide their health decisions.
The cost of the Vitamin B6 Pyridoxine Test at DNA Labs UAE is 2110 AED. This price reflects the comprehensive service provided, including the expertise of the medical professionals, the use of advanced testing technologies, and the high standards of laboratory analysis. Patients looking to undergo this test can expect a straightforward procedure requiring a simple blood sample, with results that provide valuable insights into their Vitamin B6 status.
