The SCA-2 Spinocerebellar Ataxia ATXN2 Gene Mutation Test is a specialized diagnostic tool offered by DNA Labs UAE, designed to identify mutations in the ATXN2 gene, which are responsible for Spinocerebellar Ataxia Type 2 (SCA-2). SCA-2 is a progressive, neurodegenerative disorder characterized by poor coordination of hands, speech, and eye movements, alongside other symptoms that worsen over time. Early detection through this genetic test can be crucial for managing the condition, enabling timely intervention and counseling for affected individuals and their families. The test is priced at 590 AED, making it accessible for those who suspect they may carry this mutation or have a family history of SCA-2, facilitating early and informed healthcare decisions.
The SCA-3 Spinocerebellar Ataxia ATXN3 Gene Mutation Test is a specialized genetic test designed to identify mutations in the ATXN3 gene, which are known to cause Spinocerebellar Ataxia Type 3 (SCA-3). SCA-3, also known as Machado-Joseph Disease, is a progressive neurodegenerative disorder characterized by a variety of symptoms including coordination and balance difficulties, spasticity, and eye movement abnormalities. The condition is inherited in an autosomal dominant manner, meaning that having a mutation in just one of the two copies of the ATXN3 gene is enough to cause the disorder.
This test is crucial for individuals with a family history of SCA-3 or those exhibiting symptoms suggestive of the condition, as it can provide a definitive diagnosis. Moreover, it can also be used for predictive testing in asymptomatic family members to determine their risk of developing the condition in the future.
The SCA-3 test is available at DNA Labs UAE, a leading provider of genetic testing services in the United Arab Emirates. The cost of the test is 590 AED, making it an accessible option for those seeking to understand their genetic health or risk of inheriting SCA-3. DNA Labs UAE employs state-of-the-art technology and highly qualified professionals to ensure accurate and reliable test results, providing individuals and families with the information needed to make informed health decisions.
The SCA-6 Spinocerebellar Ataxia CACNA1A Gene Mutation Test is a specialized diagnostic procedure offered by DNA Labs UAE, aimed at detecting mutations in the CACNA1A gene, which are associated with Spinocerebellar Ataxia Type 6 (SCA-6). SCA-6 is a genetic neurological disorder characterized by progressive loss of coordination, gait abnormalities, and speech difficulties, among other symptoms. This condition is inherited in an autosomal dominant manner, meaning a mutation in just one of the two copies of the gene can cause the disorder.
The test is crucial for individuals with a family history of SCA-6 or those showing symptoms of the condition, as it helps in confirming the diagnosis, enabling early intervention and management of the disease. It involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed in the laboratory to identify any mutations in the CACNA1A gene.
DNA Labs UAE offers this test at a cost of 590 AED. By providing this service, DNA Labs UAE contributes significantly to the early detection and management of Spinocerebellar Ataxia Type 6, thereby improving the quality of life for affected individuals and their families.
The "SCA-7 Spinocerebellar Ataxia ATXN7 Gene Mutation Test" is a specialized genetic test designed to identify mutations in the ATXN7 gene, which are known to cause Spinocerebellar Ataxia Type 7 (SCA-7). SCA-7 is a rare, inherited neurological disorder characterized by progressive ataxia, or loss of coordination and balance, as well as visual impairments due to degeneration of the cerebellum and other parts of the brain. This test is crucial for individuals with a family history of the disorder or those exhibiting symptoms, as it can confirm a diagnosis, allowing for better management of the condition and genetic counseling.
The test involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed in the laboratory for the presence of specific mutations in the ATXN7 gene that are responsible for SCA-7. This genetic testing is an important step in understanding the risk of passing the condition to future generations and can aid in making informed decisions about family planning.
In the United Arab Emirates, this test is available at DNA Labs UAE, a facility known for its state-of-the-art genetic testing services. The cost of the SCA-7 Spinocerebellar Ataxia ATXN7 Gene Mutation Test is 590 AED, making it accessible for individuals seeking genetic testing for this condition. By opting for this test at DNA Labs UAE, patients can expect reliable results, professional counseling, and comprehensive support throughout the testing process.
The Sjogren's Syndrome Antibodies Test is a diagnostic assessment used to detect the presence of specific antibodies associated with Sjogren's Syndrome, an autoimmune disorder. This syndrome is characterized by its primary symptoms, which include dry eyes and dry mouth, but it can also affect other parts of the body, including the joints, thyroid, kidneys, liver, lungs, skin, and nerves. The presence of specific antibodies, such as Anti-SSA (Ro) and Anti-SSB (La), is a key indicator of Sjogren's Syndrome. The test is crucial for the accurate diagnosis and management of this condition.
At DNA Labs UAE, this specialized test is available for 590 AED. The lab is equipped with state-of-the-art technology to ensure accurate and reliable results. Conducting the test in a controlled environment under the supervision of qualified professionals guarantees that the results are precise, which is essential for the correct diagnosis and subsequent treatment plan for patients suffering from Sjogren's Syndrome. This test is an important step towards managing the symptoms and improving the quality of life for individuals affected by this autoimmune disorder.
The Steroid Panel 21-Hydroxylase Deficiency Test is a specialized diagnostic tool used to detect 21-Hydroxylase Deficiency, a common cause of Congenital Adrenal Hyperplasia (CAH). This condition affects the adrenal glands' ability to produce cortisol and aldosterone, leading to an imbalance in steroid hormones. The test specifically measures the levels of certain steroids in the blood that are affected by the activity of the 21-hydroxylase enzyme. Identifying this deficiency is crucial for appropriate treatment and management of the condition.
Administered at DNA Labs UAE, a reputable facility known for its comprehensive range of genetic and molecular diagnostics, the test ensures accuracy and reliability. The cost of the Steroid Panel 21-Hydroxylase Deficiency Test is 590 AED, making it accessible for individuals seeking detailed insights into their adrenal function and potential genetic conditions affecting their steroid hormone production.
The Testosterone Total Ultrasensitive Test, available at DNA Labs UAE for a cost of 590 AED, is a highly sensitive diagnostic tool designed to accurately measure the total testosterone levels in the blood. This test is particularly useful for individuals who have lower than expected levels of testosterone, allowing for the detection of subtle variations that standard testosterone tests might miss. By utilizing advanced testing methodologies, the ultrasensitive test can provide more precise results, aiding in the diagnosis and management of conditions related to hormonal imbalances, such as hypogonadism, infertility, and certain types of tumors. DNA Labs UAE, known for its commitment to quality and accuracy, ensures that patients receive reliable and timely results, making the Testosterone Total Ultrasensitive Test an essential tool for those needing a comprehensive evaluation of their testosterone levels.
The Tetanus Toxoid Antibody IgG Test is a diagnostic tool used to measure the level of antibodies against the tetanus toxin in the blood. This test is crucial for determining an individual's immunity to tetanus, a serious bacterial infection that affects the nervous system and can lead to muscle stiffness, seizures, and even death if left untreated. The presence of IgG antibodies against the tetanus toxoid indicates prior vaccination or exposure to the bacteria, thereby providing a measure of the body's immune response and protection level against the disease.
In the United Arab Emirates, this test is available at DNA Labs UAE, a leading laboratory known for its advanced diagnostic services. The cost of the Tetanus Toxoid Antibody IgG Test at DNA Labs UAE is 590 AED. This test is particularly recommended for individuals who are at risk of tetanus exposure, those planning to travel to areas where tetanus is common, or anyone who requires a booster dose of the tetanus vaccine. It ensures that individuals have adequate immunity and helps in making informed decisions regarding vaccination.
The TORCH Panel IgG and IgM Test is a comprehensive screening tool designed to detect the presence of antibodies (IgG and IgM) against a group of infectious diseases in the blood. These diseases include Toxoplasmosis, Rubella, Cytomegalovirus (CMV), and Herpes Simplex Virus (HSV), collectively known as TORCH. The test is crucial for pregnant women, as infections caused by these pathogens can lead to serious health issues for both the mother and the fetus, including birth defects, premature birth, and miscarriage.
The test differentiates between IgG and IgM antibodies. IgG antibodies indicate past exposure and possible immunity to the infection, while IgM antibodies suggest a recent or current infection. This distinction helps healthcare providers to assess the risk and implement appropriate management strategies to protect maternal and fetal health.
At DNA Labs UAE, the TORCH Panel IgG and IgM Test is available for 590 AED. The facility ensures accurate and reliable testing services, using advanced diagnostic technologies to provide timely results. This test is an essential part of prenatal care, enabling early detection and intervention for infections that could potentially impact pregnancy outcomes.
The Antenatal Panel 1 Test is a comprehensive screening conducted during pregnancy to ensure the health and well-being of both the expectant mother and the unborn child. This panel typically includes tests for various conditions and infections that could potentially affect the pregnancy or the baby's health. It may cover screenings for anemia, diabetes, infectious diseases (such as hepatitis B, syphilis, HIV), and other conditions relevant to the prenatal period.
At DNA Labs UAE, the Antenatal Panel 1 Test is offered for 590 AED. DNA Labs UAE is known for its state-of-the-art facilities and adherence to high-quality standards in medical testing. The test is conducted by healthcare professionals who specialize in prenatal care, ensuring accurate and reliable results. This screening is crucial for early detection of potential health issues, allowing for timely intervention and management to safeguard the health of both mother and child during pregnancy.
