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DPYD Gene Dihydropyrimidine dehydrogenase deficiency Genetic Test Cost
The DPYD gene dihydropyrimidine dehydrogenase deficiency genetic test is a specialized diagnostic tool designed to identify mutations in the DPYD gene, which is crucial for the proper metabolism of certain chemotherapy drugs, such as 5-fluorouracil (5-FU) and capecitabine. Individuals with a deficiency in the dihydropyrimidine dehydrogenase (DPD) enzyme, which is encoded by the DPYD gene, may experience severe or life-threatening toxicity when treated with these medications. The test aims to guide healthcare providers in customizing cancer treatment plans, ensuring the selection of safer and more effective chemotherapy options based on the patient's genetic makeup. Performed at DNA Labs UAE, a leading facility in genetic diagnostics, the test offers a comprehensive analysis of the DPYD gene to detect any mutations that could indicate a risk of DPD deficiency. The cost of the test is set at 4400 AED, reflecting the intricate processes and sophisticated technology involved in providing accurate and reliable results. By identifying individuals at risk, the DPYD gene dihydropyrimidine dehydrogenase deficiency genetic test plays a critical role in personalized medicine, enhancing the safety and efficacy of cancer treatments.
DMGDH Gene Dimethylglycine dehydrogenase deficiency Genetic Test Cost
The DMGDH gene is responsible for encoding the enzyme dimethylglycine dehydrogenase, which plays a crucial role in the metabolism of choline-derived compounds. Deficiency in this enzyme leads to a rare metabolic disorder characterized by elevated levels of dimethylglycine in the blood. This condition can result in a variety of symptoms, including developmental delays, muscular hypotonia, and in some cases, seizures. To diagnose this condition, a genetic test can be performed that specifically looks for mutations in the DMGDH gene. This test is critical for confirming the diagnosis, understanding the severity of the enzyme deficiency, and guiding treatment plans. It involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed for mutations in the DMGDH gene. In the United Arab Emirates, DNA Labs UAE offers this specialized genetic test for DMGDH gene deficiency. The cost of the test is 4400 AED. DNA Labs UAE is equipped with state-of-the-art technology and staffed by professionals with expertise in genetic testing, ensuring accurate and reliable results. This test is a valuable resource for families seeking answers to unexplained symptoms related to metabolic disorders and provides a foundation for personalized treatment strategies.
DYM Gene Dyggve-Melchior-Clausen disease Genetic Test Cost
The DYM gene Dyggve-Melchior-Clausen (DMC) disease genetic test is a specialized diagnostic procedure offered by DNA Labs UAE, aimed at identifying mutations in the DYM gene, which are responsible for Dyggve-Melchior-Clausen disease. This rare genetic disorder is characterized by skeletal abnormalities, short trunk dwarfism, and, in some cases, developmental delays. The test plays a crucial role in the early detection and management of the condition, enabling healthcare providers to devise appropriate treatment and intervention strategies. Conducted in a state-of-the-art facility, the test ensures accuracy and reliability in results. The cost of the test is set at 4400 AED, reflecting the comprehensive nature of the analysis and the advanced technology employed in the testing process.
CYP2B6 Gene Efavirenz poor metabolism of Genetic Test Cost
The CYP2B6 Gene Efavirenz Poor Metabolism Genetic Test is a specialized diagnostic assessment available at DNA Labs UAE, designed to evaluate an individual's ability to metabolize Efavirenz, a medication commonly used in the treatment of HIV. This test focuses on analyzing the CYP2B6 gene, which plays a critical role in the metabolism of Efavirenz. Variations in this gene can lead to poor metabolism of the drug, potentially resulting in suboptimal treatment outcomes or increased side effects. Understanding an individual's genetic predisposition to metabolize Efavirenz can help healthcare providers tailor medication regimens that are more effective and have fewer side effects, leading to improved patient care. The test is priced at 4400 AED and is conducted in the state-of-the-art facilities of DNA Labs UAE, ensuring accurate and reliable results. This genetic testing is a valuable tool for personalized medicine, offering insights that can significantly impact the management of HIV treatment.
TMPRSS15 Gene Enterokinase deficiency Genetic Test Cost
The TMPRSS15 gene is responsible for encoding the enzyme enterokinase, which plays a crucial role in the digestive system by activating pancreatic digestive enzymes. A deficiency in this enzyme due to mutations in the TMPRSS15 gene can lead to a variety of digestive issues and malabsorption disorders. To diagnose this condition, a genetic test can be conducted to identify mutations in the TMPRSS15 gene that may lead to enterokinase deficiency. At DNA Labs UAE, a specialized TMPRSS15 Gene Enterokinase Deficiency Genetic Test is available for individuals who may be experiencing symptoms related to digestive enzyme deficiencies or for those who have a family history of related conditions. This test involves analyzing the patient's DNA to identify any genetic variations in the TMPRSS15 gene that could affect the production or function of enterokinase. The cost of the TMPRSS15 Gene Enterokinase Deficiency Genetic Test at DNA Labs UAE is 4400 AED. The process is straightforward and requires a sample of the patient's DNA, typically obtained through a blood draw or cheek swab. Results from this test can provide valuable information for diagnosing enterokinase deficiency, guiding treatment options, and offering insight into the genetic risk for family members.
SLC16A1 Gene Erythrocyte lactate transporter defect Genetic Test Cost
The SLC16A1 gene is crucial for encoding a protein that functions as a lactate transporter in erythrocytes (red blood cells). A defect in this gene can lead to an impaired ability of red blood cells to transport lactate, which may result in various metabolic issues and clinical symptoms. Genetic testing for the SLC16A1 gene erythrocyte lactate transporter defect is an important diagnostic tool for identifying mutations within this gene that could lead to such transporter deficiencies. DNA Labs UAE offers a comprehensive genetic test aimed at detecting mutations in the SLC16A1 gene, helping in the diagnosis of related metabolic conditions. The test involves collecting a DNA sample, typically through a blood draw, and analyzing the genetic material for specific mutations associated with the lactate transporter defect. This precise genetic testing can provide valuable information for the diagnosis, management, and treatment planning for individuals suspected of having this genetic defect. The cost of the SLC16A1 gene erythrocyte lactate transporter defect genetic test at DNA Labs UAE is 4400 AED. This investment covers the expenses associated with the sophisticated laboratory techniques and professional expertise required to accurately identify mutations in the SLC16A1 gene. For patients and healthcare providers, this genetic test is a crucial step towards understanding and managing conditions related to the erythrocyte lactate transporter defect.
GLA Gene Fabry disease Genetic Test Cost
The GLA Gene Fabry Disease Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, designed to detect mutations in the GLA gene, which are responsible for causing Fabry disease. Fabry disease is a rare genetic disorder that impacts various organs and bodily systems, leading to a wide range of symptoms including pain, kidney failure, heart issues, and stroke. The condition is inherited in an X-linked manner, meaning it predominantly affects males, though females can also be carriers and exhibit symptoms. The test involves a detailed analysis of the GLA gene to identify any genetic mutations that may be indicative of Fabry disease. This is crucial for the early diagnosis and management of the condition, allowing for timely intervention and treatment strategies to mitigate the impact of the disease on the individual's health. The cost of the GLA Gene Fabry Disease Genetic Test at DNA Labs UAE is 4400 AED. Given the specialized nature of the test and its potential to significantly influence the management of Fabry disease, it represents a valuable investment in personal health for those at risk or exhibiting symptoms suggestive of this genetic disorder.
F2 Gene Factor II deficiency Genetic Test Cost
The F2 Gene Factor II deficiency genetic test is a specialized diagnostic procedure designed to detect mutations in the F2 gene, which is responsible for the production of prothrombin (factor II) - a protein crucial for proper blood clotting. A deficiency or abnormality in Factor II can lead to either an increased risk of blood clots (thrombosis) or a bleeding disorder, depending on the nature of the mutation. This test is particularly important for individuals with a personal or family history of blood clotting disorders, as it can provide vital information for managing and treating the condition. Conducted at DNA Labs UAE, a leading facility in genetic testing, the test offers a comprehensive analysis of the F2 gene to identify any genetic anomalies that may contribute to clotting disorders. The cost of the F2 Gene Factor II deficiency genetic test is 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify mutations in the gene. By opting for this test, patients can gain valuable insights into their genetic makeup, enabling them and their healthcare providers to make informed decisions about their health management and preventive measures against potential complications associated with Factor II deficiency.
