The Placental Growth Factor (PlGF) Test is a vital diagnostic tool used in assessing the risk and monitoring of certain conditions during pregnancy, such as preeclampsia. PlGF is a protein associated with placental development, and abnormal levels can indicate potential complications with the pregnancy. This test measures the amount of PlGF in the blood, providing crucial information for the early detection and management of conditions that could affect both the mother and the fetus's health.
At DNA Labs UAE, the PlGF Test is offered at a cost of 590 AED. DNA Labs UAE is equipped with state-of-the-art facilities and experienced professionals to ensure accurate and reliable test results. This test is particularly recommended for pregnant women who are at risk of developing preeclampsia, as it can help in taking preventive measures or interventions at an early stage. By opting for this test, expectant mothers can take a proactive step towards ensuring a healthier pregnancy outcome.
The "SCA-1 Spinocerebellar Ataxia ATXN1 Gene Mutation Test" is a specialized genetic test offered by DNA Labs UAE, designed to identify mutations in the ATXN1 gene, which are linked to Spinocerebellar Ataxia Type 1 (SCA-1). SCA-1 is a rare, inherited neurological disorder characterized by progressive loss of coordination, difficulty walking, and speech problems, among other symptoms. This condition is caused by a specific genetic mutation in the ATXN1 gene, which affects the brain's cerebellum and spinal cord.
The test is crucial for individuals with a family history of SCA-1 or those exhibiting symptoms, as it can provide definitive diagnosis and help in managing the condition. Early detection through this genetic testing can also inform family planning decisions for those carrying the mutation. The procedure involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed for the presence of the ATXN1 mutation.
At DNA Labs UAE, the cost of the SCA-1 Spinocerebellar Ataxia ATXN1 Gene Mutation Test is 590 AED. The test is conducted in a state-of-the-art laboratory by skilled professionals, ensuring accurate and reliable results. Individuals seeking this test can expect a thorough and confidential service, with support and guidance provided throughout the testing process.
The SCA-12 Spinocerebellar Ataxia PPP2R2B Gene Mutation Test is a specialized genetic test designed to identify mutations in the PPP2R2B gene, which are associated with Spinocerebellar Ataxia Type 12 (SCA-12). SCA-12 is a progressive, neurodegenerative disorder characterized by tremors, difficulty with movement coordination (ataxia), and other neurological symptoms. This condition is inherited in an autosomal dominant pattern, meaning that a mutation in just one copy of the gene in each cell is sufficient to cause the disorder.
The test is conducted by DNA Labs UAE, a leading provider of genetic testing services in the United Arab Emirates. Utilizing advanced genetic sequencing technologies, the test accurately detects the presence of specific mutations in the PPP2R2B gene that are known to cause SCA-12. This information is crucial for affected individuals and their families for several reasons. It can confirm a diagnosis of SCA-12, inform treatment and management strategies, and provide valuable information for family planning and genetic counseling.
The cost of the SCA-12 Spinocerebellar Ataxia PPP2R2B Gene Mutation Test at DNA Labs UAE is 590 AED. Given the specialized nature of this test and its importance in the diagnosis and management of SCA-12, it represents a critical investment in the health and well-being of individuals showing symptoms of or at risk for this condition.
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.
