Search Results for: name
ABCB4 Gene Cholestasis progressive intrahepatic type 3 Genetic Test Cost
The ABCB4 gene plays a crucial role in the body's ability to transport bile acids from the liver to the gallbladder, a process essential for the digestion and absorption of fats. Mutations in the ABCB4 gene can lead to a condition known as progressive familial intrahepatic cholestasis type 3 (PFIC3), a rare genetic disorder characterized by impaired bile flow (cholestasis) that progresses to liver disease. Symptoms of PFIC3 can include jaundice, itching, and potentially more severe liver-related issues over time. To diagnose PFIC3, a genetic test focusing on the ABCB4 gene can be conducted. In the UAE, DNA Labs UAE offers this specific genetic testing service. The test is designed to detect mutations in the ABCB4 gene that are associated with the development of PFIC3. By identifying these mutations, healthcare providers can confirm a diagnosis of PFIC3, enabling them to tailor treatment plans more effectively for affected individuals. The cost of the ABCB4 Gene Cholestasis progressive intrahepatic type 3 Genetic Test at DNA Labs UAE is 3200 AED. This price includes the process of collecting a DNA sample, usually through a blood draw or cheek swab, and the subsequent analysis of the sample to identify any mutations in the ABCB4 gene. Once the test is completed, a detailed report is provided, offering crucial insights into the patient's genetic predisposition to PFIC3. This information can be invaluable for making informed decisions regarding the management and treatment of the condition.
ATP8B1 Gene Cholestasis benign recurrent intrahepatic Genetic Test Cost
The ATP8B1 gene plays a significant role in the normal functioning of the liver, and mutations in this gene can lead to a condition known as benign recurrent intraheptic cholestasis (BRIC). BRIC is characterized by episodes of liver dysfunction that can cause jaundice, itching, and elevated liver enzymes, but typically does not lead to long-term liver damage. Genetic testing for mutations in the ATP8B1 gene can provide crucial information for diagnosing this condition, guiding treatment options, and offering insights into the prognosis. At DNA Labs UAE, a specialized genetic test is available for identifying mutations in the ATP8B1 gene that are associated with benign recurrent intraheptic cholestasis. The test is conducted using a blood sample, with results typically available within a few weeks. The cost of the test is 3200 AED. This testing can be particularly valuable for individuals who have experienced symptoms suggestive of BRIC, or for family members of individuals diagnosed with the condition, as it can help in understanding the genetic basis of the disease and in making informed decisions about management and monitoring.
ATP8B1 Gene Cholestasis intrahepatic of pregnancy type 1 Genetic Test Cost
The ATP8B1 gene plays a crucial role in maintaining proper liver function. Mutations in this gene can lead to a condition known as intrahepatic cholestasis of pregnancy type 1 (ICP1), a liver disorder that occurs during pregnancy. This condition can cause severe itching in the expectant mother and, in some cases, lead to complications for the baby. To diagnose this genetic predisposition, DNA Labs UAE offers a specific genetic test targeting the ATP8B1 gene. This test is essential for women with a family history of ICP1 or those who have experienced symptoms related to this condition in previous pregnancies. Early detection through this genetic test can help in managing the symptoms more effectively and in making informed decisions regarding pregnancy. The test cost is set at 4400 AED, reflecting the specialized nature of the analysis and the sophisticated technology used to identify mutations in the ATP8B1 gene accurately. By choosing to undergo this test at DNA Labs UAE, patients can expect reliable results backed by expert analysis, helping to ensure the well-being of both mother and child during pregnancy.
LIPA Gene Cholesteryl ester storage disease Genetic Test Cost
The LIPA Gene Cholesteryl Ester Storage Disease Genetic Test is a specific diagnostic tool used to identify mutations in the LIPA gene, which are responsible for causing Cholesteryl Ester Storage Disease (CESD). CESD is a rare lipid metabolism disorder characterized by the accumulation of cholesteryl esters and triglycerides in various tissues of the body, leading to liver disease, lipid abnormalities, and potentially cardiovascular disease. This test is crucial for confirming the diagnosis, allowing for early intervention and management of the condition. Performed at DNA Labs UAE, a reputable facility known for its advanced genetic testing capabilities, the test involves analyzing the patient's DNA to look for mutations in the LIPA gene. The process is straightforward, requiring a simple blood sample from the patient. DNA Labs UAE ensures accurate and reliable results, employing the latest in genetic testing technology. The cost of the LIPA Gene Cholesteryl Ester Storage Disease Genetic Test is set at 4400 AED. While the price might seem significant, the value of obtaining a precise diagnosis cannot be overstated, as it opens the door to targeted treatments and personalized management plans for affected individuals. This test is a vital resource for families and individuals facing the challenges of CESD, providing them with the information needed to tackle the disease more effectively.
SAR1B Gene Chylomicron retention disease Genetic Test Cost
The SAR1B gene plays a critical role in the proper digestion and absorption of fats and fat-soluble vitamins in the body. Mutations in this gene can lead to Chylomicron Retention Disease (CRD), a rare genetic disorder characterized by the inability to properly absorb dietary fats, leading to symptoms such as failure to thrive, steatorrhea (fatty stools), and fat-soluble vitamin deficiencies in affected individuals. To diagnose this condition, a genetic test targeting the SAR1B gene can be conducted. This test involves analyzing the DNA to identify mutations in the SAR1B gene that are known to cause CRD. It is a crucial step for confirming the diagnosis, understanding the disease's progression, and managing the patient's condition effectively through dietary modifications and vitamin supplementation. At DNA Labs UAE, this specific genetic test for the SAR1B gene Chylomicron Retention Disease is available. The cost of the test is 4400 AED. The process involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed in the laboratory for the presence of mutations in the SAR1B gene. Results from this test can provide essential information for the diagnosis and management of CRD, enabling healthcare providers to offer targeted treatment and dietary recommendations to improve the quality of life for affected individuals.
SLC25A13 Gene Citrin deficiency Genetic Test Cost
The SLC25A13 gene is responsible for encoding a protein called citrin, which plays a crucial role in the urea cycle and the metabolism of amino acids and carbohydrates in the body. A deficiency in citrin caused by mutations in the SLC25A13 gene can lead to a range of metabolic disorders, including Neonatal Intrahepatic Cholestasis caused by Citrin Deficiency (NICCD) and Citrullinemia Type II. These conditions can manifest with symptoms such as jaundice, failure to thrive, liver dysfunction, and in more severe cases, neurological issues. To diagnose citrin deficiency and related metabolic disorders accurately, genetic testing of the SLC25A13 gene is employed. This test involves analyzing the DNA to identify mutations in the SLC25A13 gene that are known to cause citrin deficiency. It is a crucial step in confirming the diagnosis, which can then guide appropriate management and treatment plans for affected individuals. In the UAE, DNA Labs offers the SLC25A13 gene citrin deficiency genetic test, providing a reliable diagnosis for those suspected of having this condition. The test cost is set at 4400 AED. By opting for this test at DNA Labs UAE, patients can expect a comprehensive analysis, ensuring accurate diagnosis and the potential for timely intervention to manage symptoms and improve quality of life.
ASS1 Gene Citrullinemia Genetic Test Cost
The ASS1 Gene Citrullinemia Genetic Test is a specialized diagnostic procedure aimed at identifying mutations in the ASS1 gene, which is pivotal for diagnosing Citrullinemia, a rare genetic disorder. Citrullinemia results from the body's inability to eliminate ammonia from the bloodstream due to a deficiency in the enzyme argininosuccinate synthetase, which is crucial for the urea cycle. This condition can lead to harmful levels of ammonia in the blood, causing severe implications for an individual's health, including neurological impairments and, if untreated, can be life-threatening. Conducted at DNA Labs UAE, a leading facility in genetic testing, the test involves collecting a DNA sample, typically through a blood draw or a cheek swab, to analyze the genetic makeup of the ASS1 gene. This comprehensive analysis helps in identifying any mutations that may lead to the dysfunction of the enzyme responsible for ammonia detoxification in the liver. The cost of the ASS1 Gene Citrullinemia Genetic Test at DNA Labs UAE is set at 4400 AED. This price reflects the sophisticated technology and expertise required to accurately diagnose this condition, ensuring that individuals receive the necessary information for proper management and treatment. Early detection through this genetic test can significantly improve the quality of life for those affected by Citrullinemia by allowing for timely interventions and personalized treatment plans.
COQ6 Gene Coenzyme Q10 deficiency type 6 Genetic Test Cost
The COQ6 gene coenzyme Q10 deficiency type 6 genetic test is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the COQ6 gene, which are associated with a rare form of coenzyme Q10 deficiency. This condition is a mitochondrial disorder that can affect multiple systems of the body, including the nervous system and the kidneys. Symptoms can vary widely among affected individuals but may include muscle weakness, seizures, developmental delays, and kidney failure. The test is crucial for the early detection and management of this condition, allowing for appropriate treatment strategies, including supplementation with coenzyme Q10 and other supportive therapies, to be implemented. This can significantly improve the quality of life for individuals with coenzyme Q10 deficiency type 6. The cost of the COQ6 gene coenzyme Q10 deficiency type 6 genetic test at DNA Labs UAE is 4400 AED. The test involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory to detect mutations in the COQ6 gene. The process is conducted by experienced professionals to ensure accurate and reliable results. Given the complexity and the specialized nature of the test, the cost reflects the extensive resources required for precise genetic analysis.