Canavan Disease Test at DNA Labs UAE
The Canavan Disease Test is a crucial genetic screening offered by DNA Labs UAE, aimed at detecting Canavan disease, a rare inherited disorder that affects the brain's ability to send and receive messages. This condition typically manifests in infancy and is characterized by a progressive degeneration of nerve cells in the brain. The test is particularly important for individuals with a family history of the disease or those of Ashkenazi Jewish descent, who are at a higher risk.
DNA Labs UAE utilizes advanced genetic testing techniques to analyze the patient's DNA for mutations in the ASPA gene, which are responsible for Canavan disease. The process is straightforward, requiring only a simple blood sample or cheek swab from the patient. The test is priced at 750 AED, making it accessible for those seeking peace of mind regarding their genetic health or planning for a family.
By opting for the Canavan Disease Test at DNA Labs UAE, individuals can gain valuable insights into their genetic makeup, enabling early intervention and management strategies for those affected by the disease. This proactive approach underscores the importance of genetic testing in modern healthcare, providing a pathway to better health outcomes and informed family planning decisions.
The Cardiac Myocardial Infarction Panel Test is a critical diagnostic tool used to assess the presence of specific markers in the blood that indicate a heart attack or myocardial infarction. This comprehensive panel measures levels of substances such as troponin, which is released into the bloodstream when the heart muscle is damaged. Early detection and quantification of these markers are vital for the timely management and treatment of myocardial infarction, potentially saving lives and reducing the risk of complications.
Offered at DNA Labs UAE, a leading diagnostic center known for its advanced medical testing technologies and expertise, this test is priced at 750 AED. The facility ensures accuracy and reliability in results, providing essential information for healthcare providers to make informed decisions regarding patient care. The Cardiac Myocardial Infarction Panel Test is a must-have for individuals experiencing symptoms of a heart attack or those at high risk, offering peace of mind and facilitating prompt medical intervention.
The Cardiometabolic Syndrome Panel Test is a comprehensive diagnostic assessment offered by DNA Labs UAE, designed to evaluate an individual's risk factors for cardiometabolic syndrome. Priced at 750 AED, this test is an essential tool in identifying the presence of metabolic abnormalities that may predispose a person to cardiovascular diseases, diabetes, stroke, and other related conditions. The panel typically includes a series of blood tests measuring glucose levels, lipid profile, blood pressure, and other markers indicative of metabolic health. By assessing these critical parameters, the test provides valuable insights into an individual’s cardiometabolic status, enabling early detection and intervention. Conducted in the state-of-the-art facilities of DNA Labs UAE, this test is a proactive step towards managing and mitigating the risk of developing cardiometabolic syndrome, promoting a healthier, more informed lifestyle.
The Chromium 24 Hour Urine Test is a diagnostic procedure conducted to measure the levels of chromium in the urine over a 24-hour period. This test is crucial for individuals who are exposed to chromium through their environment or occupation, as it helps in assessing chromium exposure and its potential health implications. Chromium is a metal that, at high levels, can pose serious health risks, including lung cancer and kidney damage. The test involves collecting all urine produced in a 24-hour period in a special container provided by the laboratory. It is a non-invasive test that provides valuable information on the body's chromium levels, aiding in the diagnosis of poisoning or monitoring exposure to this metal.
At DNA Labs UAE, the Chromium 24 Hour Urine Test is offered at a cost of 750 AED. DNA Labs UAE is known for its state-of-the-art facilities and adherence to high-quality standards in medical testing. Conducting the test in such a reputable lab ensures accurate and reliable results, which are crucial for the effective management of health risks associated with chromium exposure.
The Succinylacetone Blood Test is a specialized diagnostic procedure designed to detect the presence of succinylacetone in the blood, which is a key marker for Tyrosinemia Type I, a rare genetic disorder. This test is crucial for early detection and management of the condition, which can lead to serious health complications if left untreated. At DNA Labs UAE, this test is conducted with precision and care, ensuring accurate results for patients. The cost of the Succinylacetone Blood Test at DNA Labs UAE is 820 AED, making it accessible for those in need of this important diagnostic service.
The Succinylacetone Urine Test is a specialized diagnostic procedure performed to detect elevated levels of succinylacetone in the urine, which can be a critical indicator of Tyrosinemia Type I, a rare genetic disorder. This condition affects how the body breaks down the amino acid tyrosine, leading to a build-up of toxic substances in the liver, kidneys, and nervous system, potentially causing serious health issues. Early detection through the Succinylacetone Urine Test can facilitate timely intervention and management strategies to mitigate the effects of this disorder.
At DNA Labs UAE, this test is meticulously conducted in a state-of-the-art laboratory setting by experienced professionals, ensuring accurate and reliable results. The cost of the Succinylacetone Urine Test is set at 820 AED, reflecting the comprehensive approach taken in the analysis and the utilization of advanced diagnostic technology to achieve precise outcomes. Opting for this test at DNA Labs UAE means accessing quality healthcare diagnostics within a supportive and efficient system, aimed at providing critical insights into one’s genetic health profile.
The Thalassemia Monitoring Panel Test is a specialized diagnostic assessment offered by DNA Labs UAE, designed to evaluate and monitor individuals diagnosed with thalassemia, a genetic blood disorder characterized by reduced hemoglobin production. This condition can lead to anemia, fatigue, and, in severe cases, organ damage. The test plays a crucial role in managing the disease effectively, helping healthcare providers tailor treatment plans to the patient's specific needs.
At a cost of 820 AED, the Thalassemia Monitoring Panel Test encompasses a comprehensive analysis of various blood parameters and genetic markers associated with thalassemia. This includes evaluating the types and levels of hemoglobin present, identifying mutations or deletions in the genes responsible for hemoglobin production, and monitoring the overall health of red blood cells. By providing detailed insights into the patient's condition, the test aids in assessing the severity of the disease, tracking its progression, and adjusting therapeutic interventions accordingly.
DNA Labs UAE, known for its advanced diagnostic facilities and expertise in genetic testing, ensures high accuracy and reliability of the Thalassemia Monitoring Panel Test. Patients and healthcare providers can expect results that offer valuable guidance in the ongoing management of thalassemia, contributing to improved patient outcomes and quality of life.
The VMA (Vanillyl Mandelic Acid) 24-Hour Urine Test is a diagnostic procedure used to measure the levels of vanillyl mandelic acid in the urine over a 24-hour period. Vanillyl mandelic acid is a metabolite of catecholamines (adrenaline and noradrenaline), which are hormones released by the adrenal glands in response to stress. This test is particularly useful in diagnosing tumors that affect catecholamine production, such as pheochromocytomas and neuroblastomas, which can lead to elevated levels of VMA.
Patients are required to collect all urine produced in a 24-hour period in a special container provided by the laboratory. This comprehensive collection method ensures a more accurate assessment of VMA levels over time, compared to a single urine sample.
The VMA 24-Hour Urine Test is available at DNA Labs UAE, a leading provider of diagnostic and genetic testing services in the United Arab Emirates. The cost of the test is 820 AED. DNA Labs UAE is known for its state-of-the-art facilities and commitment to providing accurate and reliable test results, making it a preferred choice for patients and healthcare providers seeking comprehensive diagnostic solutions.
The VMA (Vanillyl Mandelic Acid) Random Urine Test is a diagnostic examination aimed at measuring the levels of vanillyl mandelic acid in the urine. This test is particularly significant as VMA is a major metabolite of catecholamines (epinephrine, norepinephrine, and dopamine), which are hormones released by the adrenal glands. High levels of VMA in urine can indicate the presence of certain medical conditions, including neuroblastoma, a type of cancer that especially affects infants and young children, and other tumors related to the nervous system.
This test does not require any special preparation, such as fasting, and can be performed at any time of the day. The process involves collecting a random urine sample, which is then analyzed by a laboratory.
In the United Arab Emirates, this specific test is available at DNA Labs UAE, a facility known for its comprehensive range of diagnostic and genetic testing services. The cost of the VMA Vanillyl Mandelic Acid Random Urine Test at DNA Labs UAE is set at 820 AED. This test is crucial for individuals who may be exhibiting symptoms or have a medical history that suggests an elevated risk of conditions affecting the adrenal glands or nervous system. By providing accurate and timely results, DNA Labs UAE plays a vital role in the diagnostic process, aiding in the early detection and management of potential health issues.
The Porphobilinogen (PBG) Qualitative Urine Test is a specialized diagnostic procedure designed to detect abnormal levels of PBG in the urine, which is a critical indicator for various types of porphyria. Porphyrias are a group of rare inherited or acquired disorders of certain enzymes in the heme biosynthesis pathway, leading to a buildup of natural chemicals that produce porphyrin in the body. Elevated levels of PBG in urine can signal an acute attack of porphyria, making this test crucial for the diagnosis and management of the condition.
Performed at DNA Labs UAE, a reputable facility known for its comprehensive range of diagnostic services, the PBG Qualitative Urine Test is conducted by collecting a urine sample from the patient. This sample is then analyzed using sophisticated laboratory techniques to detect the presence and concentration of porphobilinogen. The results from this test can provide essential information for the diagnosis, treatment planning, and monitoring of individuals suspected of having or known to have porphyria.
The cost of the Porphobilinogen Qualitative Urine Test at DNA Labs UAE is 820 AED. Given the specialized nature of this test and its importance in diagnosing potentially serious conditions, it represents a critical investment in one's health for individuals showing symptoms or with a family history of porphyria. It is always recommended to consult with a healthcare provider to understand the need for this test and its implications fully.
