Symptoms of Arthrogryposis Arthrogryposis, also known as arthrogryposis multiplex congenita (AMC), is a condition characterized by multiple joint contractures found throughout the body at birth. The term is derived from Greek, meaning ‘curved or hooked joints’. The condition is not a single disease but a symptom complex that spans over 300 specific diseases. The primary
The Galactose Quantitative Plasma Test is a diagnostic procedure designed to measure the levels of galactose in the plasma. Galactose is a type of sugar found in milk and other dairy products, fruits, and vegetables. It is crucial for diagnosing and managing disorders related to galactose metabolism, such as Galactosemia, a rare genetic disorder that prevents the proper metabolism of galactose leading to its accumulation in the body, which can cause liver damage, cataracts, and brain damage if not treated promptly.
This test is particularly important for newborns and infants who exhibit symptoms of galactosemia, including jaundice, vomiting, and feeding difficulties, as early diagnosis and treatment can prevent serious health complications. The test involves drawing a small sample of blood from the patient, which is then analyzed to determine the concentration of galactose in the plasma.
At DNA Labs UAE, the Galactose Quantitative Plasma Test is available for a cost of 370 AED. DNA Labs UAE is equipped with state-of-the-art facilities and employs advanced testing methodologies to ensure accurate and reliable results. The lab is staffed by experienced professionals who are committed to providing high-quality diagnostic services. This test is an essential tool in the management and treatment of galactose-related disorders, helping to ensure the well-being of affected individuals.
The Galactosemia Panel 1 Test is a crucial diagnostic tool used to detect galactosemia, a rare genetic disorder that affects an individual's ability to metabolize galactose, a simple sugar found in milk and dairy products. This condition, if left untreated, can lead to serious complications such as liver damage, cataracts, intellectual disability, and even death in infants. The test is designed to identify various forms of the disease by examining specific genes known to be associated with galactosemia.
Performed at DNA Labs UAE, a leading facility in genetic testing and analysis, the Galactosemia Panel 1 Test offers a comprehensive screening for the most common and severe forms of galactosemia, including GALT (galactose-1-phosphate uridyltransferase) deficiency, which is the most prevalent type. By analyzing the patient's DNA, the test can identify mutations in the genes responsible for galactose metabolism, providing essential information for diagnosis and management of the condition.
The cost of the Galactosemia Panel 1 Test at DNA Labs UAE is 570 AED. This investment in health enables early detection and intervention, which are critical in preventing the potentially life-threatening complications associated with galactosemia. Early diagnosis through the Galactosemia Panel 1 Test allows for the implementation of a galactose-free diet, significantly improving the quality of life and long-term outcomes for individuals with this genetic disorder.
The Hepatitis B Immunity Screen Test is a crucial diagnostic tool offered by DNA Labs UAE, designed to determine an individual's immunity status against the Hepatitis B virus (HBV). Priced at 590 AED, this test specifically looks for the presence of antibodies produced in response to a previous infection or vaccination against HBV, indicating whether a person has developed immunity to the virus. The procedure involves a simple blood draw, and the results can help healthcare professionals advise on the necessity of vaccination or booster shots, especially for those at higher risk of exposure. This test is essential for ensuring personal health safety and for public health strategies aimed at controlling the spread of Hepatitis B, a potentially life-threatening liver infection.
The Orotic Acid Test is a specialized diagnostic assessment conducted at DNA Labs UAE, designed to measure the levels of orotic acid in the urine. Orotic acid is a crucial compound in the body, involved in the synthesis of pyrimidines, an essential component of DNA and RNA. Abnormal levels of orotic acid can indicate a variety of metabolic disorders, including hereditary orotic aciduria and issues related to the urea cycle, among others. These conditions can lead to developmental delays, growth issues, and other serious health problems if not diagnosed and treated promptly.
DNA Labs UAE, a leading facility in genetic and molecular diagnostics, offers the Orotic Acid Test for a cost of 820 AED. The test is conducted using advanced laboratory techniques to ensure accurate and reliable results. It is typically recommended for individuals who show symptoms of metabolic disorders or have a family history of such conditions. The process involves collecting a urine sample from the patient, which is then analyzed by specialized laboratory technicians.
This test plays a crucial role in the early detection and management of metabolic disorders, enabling healthcare providers to develop an appropriate treatment plan to address the specific needs of the patient. With its state-of-the-art technology and expert team, DNA Labs UAE provides a crucial service in the field of genetic and metabolic health.
The Lamotrigine Test is a specialized diagnostic procedure aimed at measuring the concentration of lamotrigine in the blood. Lamotrigine is a medication primarily used in the treatment of epilepsy and bipolar disorder, helping to control seizures and mood swings. Monitoring its levels is crucial to ensure therapeutic efficacy and to avoid toxicity or adverse reactions.
DNA Labs UAE offers this precise testing service for individuals prescribed lamotrigine, providing essential insights into how the patient metabolizes and responds to the medication. This can assist healthcare providers in adjusting dosages for optimal outcomes. The test is priced at 810 AED, reflecting the advanced technology and expertise involved in conducting this analysis. With DNA Labs UAE, patients and physicians can expect reliable results that support effective and personalized treatment plans.
The HIV RNA PCR Qualitative Test is a diagnostic tool used to detect the presence of the Human Immunodeficiency Virus (HIV) RNA in the blood. Unlike tests that look for antibodies or antigens, this test directly identifies the virus's genetic material, making it possible to detect HIV shortly after infection, even before the body has produced antibodies. This early detection capability is crucial for prompt intervention and management of the condition.
Performed at DNA Labs UAE, a leading facility known for its advanced diagnostic technologies and expertise, the test offers a high degree of accuracy and reliability. The cost of the test is 1000 AED, an investment in health that allows for early and precise diagnosis. Early diagnosis through the HIV RNA PCR Qualitative Test can significantly impact treatment outcomes and reduce the risk of HIV transmission to others.
Prader-Willi Syndrome (PWS) is a rare genetic disorder characterized by a range of physical, mental, and behavioral problems including chronic hunger, poor muscle tone, and developmental delays. To accurately diagnose this condition, the Prader-Willi Syndrome FISH (Fluorescence In Situ Hybridization) test is employed, which is a sophisticated genetic test designed to detect abnormalities specific to the chromosome 15 region associated with PWS.
The FISH test involves using fluorescent probes that bind to specific parts of chromosomes, making it possible to visualize genetic abnormalities under a microscope. This method is highly effective in identifying the deletion or uniparental disomy (UPD) of chromosome 15, which are common genetic markers of Prader-Willi Syndrome.
In the United Arab Emirates, DNA Labs UAE is a reputable facility that offers the Prader-Willi Syndrome FISH Test. The test is priced at 1050 AED, providing a crucial diagnostic tool for families and physicians dealing with the potential diagnosis of PWS. The results from this test can help in planning appropriate management and therapeutic strategies for individuals diagnosed with Prader-Willi Syndrome, ultimately improving their quality of life.
The Gabapentin Test is a specialized diagnostic procedure aimed at detecting and measuring the levels of Gabapentin in the body. Gabapentin, a medication commonly prescribed for the management of neuropathic pain, seizures, and other conditions, requires careful monitoring to ensure therapeutic efficacy and avoid potential side effects. The test is particularly relevant for individuals undergoing treatment with Gabapentin, enabling healthcare providers to tailor dosages accurately and optimize treatment plans.
Conducted at DNA Labs UAE, a leading facility renowned for its advanced diagnostic services and adherence to international standards, the Gabapentin Test ensures precision and reliability. The test cost is set at 1400 AED, reflecting the sophisticated technology and expertise involved in the analysis. By choosing DNA Labs UAE for the Gabapentin Test, patients and healthcare providers can expect comprehensive support, from sample collection to detailed result interpretation, facilitating effective management of conditions requiring Gabapentin therapy.
The Fish - Prader Willi Syndrome SNRPN Test is a specialized genetic examination aimed at diagnosing Prader-Willi Syndrome (PWS), a complex genetic disorder characterized by a variety of physical, mental, and behavioral features. This test specifically targets the SNRPN gene, which plays a crucial role in the development of PWS. It employs fluorescence in situ hybridization (FISH) technology to detect abnormalities associated with the SNRPN gene, such as deletions or uniparental disomy, which are common genetic mechanisms underlying Prader-Willi Syndrome.
Conducted at DNA Labs UAE, a leading facility in genetic testing, the test provides a reliable diagnosis for families seeking answers to developmental delays, feeding difficulties in infancy, followed by excessive eating and weight gain in older children and adults, among other symptoms associated with PWS. The cost of the test is 1500 AED, making it a valuable investment for those in need of a definitive diagnosis, which can lead to early intervention and management strategies tailored to the specific needs of individuals with Prader-Willi Syndrome.
