Search Results for: results
GYS1 Gene Glycogen storage disease type 0 muscle Genetic Test Cost
The GYS1 Gene Glycogen Storage Disease Type 0 (GSD0) muscle genetic test is a specialized diagnostic procedure available at DNA Labs UAE, aimed at detecting mutations in the GYS1 gene. These mutations are responsible for the rare metabolic disorder known as Glycogen Storage Disease Type 0, which affects the muscle form of the condition. GSD0 is characterized by an inability to properly store glycogen in muscles, leading to various symptoms including muscle weakness, cramps, and potentially serious health complications. The test involves a detailed analysis of the patient's DNA to identify any genetic abnormalities in the GYS1 gene that might indicate the presence of the disease. This is crucial for early detection, accurate diagnosis, and the management of symptoms through appropriate treatment and lifestyle adjustments. At DNA Labs UAE, the test is priced at 4400 AED. The cost reflects the comprehensive nature of the genetic analysis, the expertise required to interpret the results accurately, and the sophisticated technology employed in the testing process. For patients suspected of having GSD0 or for those with a family history of the condition, this test provides essential insights into their genetic health, enabling informed decisions about their care and management.
PGAM2 Gene Glycogen storage disease type 10 Genetic Test Cost
The PGAM2 gene is associated with Glycogen Storage Disease Type X (also known as Glycogen Storage Disease Type 10), a metabolic disorder that affects muscle function. This condition is characterized by a deficiency in the enzyme phosphoglycerate mutase, which is crucial for glycogen metabolism in muscle tissues. Symptoms can include muscle cramps, exercise intolerance, and myoglobinuria, potentially leading to kidney damage in severe cases. Genetic testing for mutations in the PGAM2 gene is a critical step in diagnosing Glycogen Storage Disease Type X. This test helps in confirming the diagnosis, understanding the disease's progression, and planning appropriate management and treatment strategies for affected individuals. At DNA Labs UAE, a specialized test for the PGAM2 gene related to Glycogen Storage Disease Type 10 is available. The cost of this genetic test is 4400 AED. Conducting this test at DNA Labs UAE ensures accurate diagnosis through state-of-the-art genetic testing technologies, provided by a team of experts in genetic disorders. This facilitates early and effective intervention, improving the quality of life for individuals with this condition.
LDHA Gene Glycogen storage disease type 11 Genetic Test Cost
The LDHA gene plays a crucial role in the metabolism of carbohydrates, specifically in the final step of anaerobic glycolysis, converting pyruvate to lactate. Mutations in this gene can lead to Glycogen Storage Disease Type XI (also known as lactate dehydrogenase A deficiency), a rare metabolic disorder characterized by an inability to adequately break down glycogen in the body. This can lead to a variety of symptoms, including muscle pain, cramps, and exercise intolerance. Genetic testing for mutations in the LDHA gene is essential for the diagnosis of Glycogen Storage Disease Type XI. This testing can help in confirming the diagnosis, understanding the disease's progression, and making informed decisions about management and treatment options. It can also provide valuable information for family planning and the assessment of risk for future offspring. DNA Labs UAE offers a comprehensive genetic test targeting the LDHA gene to diagnose Glycogen Storage Disease Type XI. The cost of the test is 4400 AED. Conducted in a state-of-the-art facility, this test provides a reliable analysis of the LDHA gene to detect mutations associated with the disease. The process involves collecting a DNA sample, usually through a blood draw or a cheek swab, which is then analyzed in the laboratory using advanced genetic sequencing techniques. Upon completion, the results offer a detailed view of the patient's genetic makeup concerning the LDHA gene, enabling healthcare providers to make informed decisions regarding the patient's condition and management. Given the complexity of genetic conditions, individuals undergoing this test are often advised to consult with a genetic counselor or a specialist in metabolic disorders to interpret the results accurately and discuss the implications for treatment and family planning.
ALDOA Gene Glycogen storage disease type 12 Genetic Test Cost
The ALDOA gene plays a crucial role in the glycolysis pathway, which is essential for energy production in cells. Mutations in the ALDOA gene can lead to Glycogen Storage Disease Type 12 (GSD XII), a rare metabolic disorder characterized by muscle weakness, fatigue, and myalgia. This condition arises from the body's inability to properly break down glycogen, a stored form of glucose, due to the deficient activity of the aldolase A enzyme. To diagnose GSD XII, a genetic test targeting the ALDOA gene can be conducted. This test is vital for confirming the diagnosis, understanding the disease's progression, and guiding treatment options. It involves analyzing the patient's DNA to identify mutations in the ALDOA gene that are responsible for the condition. In the UAE, this specific genetic test for GSD XII can be performed at DNA Labs UAE, a reputable facility known for its advanced genetic testing services. The cost of the test is set at 4400 AED. Opting for this test at DNA Labs UAE ensures that patients receive accurate and reliable results, thanks to the lab's use of cutting-edge technology and adherence to international standards in genetic testing. This test is a crucial step for affected individuals and their families in managing the condition effectively and improving the quality of life for those diagnosed with Glycogen Storage Disease Type 12.
PGM1 Gene Glycogen storage disease type 14 Genetic Test Cost
The PGM1 Gene Glycogen Storage Disease Type 14 Genetic Test is a specialized diagnostic assessment conducted to identify mutations in the PGM1 gene, which are responsible for Glycogen Storage Disease Type 14 (GSD XIV). This condition is a rare genetic disorder affecting the body's ability to metabolize glycogen properly, leading to various symptoms such as muscle weakness, liver dysfunction, and in some cases, cardiomyopathy. The test aims to provide a definitive diagnosis by analyzing the patient's DNA for specific genetic alterations in the PGM1 gene, enabling targeted management and treatment strategies for those affected. Performed at DNA Labs UAE, a leading facility in genetic diagnostics, the test offers a comprehensive analysis with the reliability of advanced genetic testing technologies. The cost for this genetic test is set at 4400 AED, reflecting the sophisticated nature of the testing process and the invaluable insights it provides for patients and their families. By opting for this test, individuals suspected of having GSD XIV can gain a clear understanding of their genetic status, facilitating informed decisions about their health and treatment options.
GYG1 Gene Glycogen storage disease type 15 Genetic Test Cost
The GYG1 gene plays a crucial role in the body's ability to store and metabolize glycogen, a key energy source for cells. Mutations in the GYG1 gene can lead to Glycogen Storage Disease Type 15 (GSD XV), a rare genetic disorder that affects muscle function and can cause muscle weakness, cramps, and exercise intolerance. To diagnose this condition, genetic testing is essential. DNA Labs UAE offers a specialized genetic test for identifying mutations in the GYG1 gene associated with GSD XV. The test is a comprehensive tool for individuals experiencing symptoms suggestive of glycogen storage diseases or for those with a family history of GSD XV seeking a definitive diagnosis. The cost of the GYG1 Gene Glycogen Storage Disease Type 15 Genetic Test is 4400 AED. This test involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory to detect any mutations in the GYG1 gene. Results from this test can provide crucial information for diagnosis, allowing for appropriate management and treatment plans to be developed. It is also valuable for family planning and understanding the risk of passing the condition to future generations. For those considering this test, it is recommended to consult with a healthcare provider or a genetic counselor to understand the implications of the results and the next steps in care and management. DNA Labs UAE ensures confidentiality and provides professional guidance throughout the testing process.
G6PC Gene Glycogen storage disease type 1A Genetic Test Cost
The G6PC gene glycogen storage disease type 1A genetic test is a specialized diagnostic procedure designed to detect mutations in the G6PC gene, which are responsible for causing glycogen storage disease type 1A (GSD1A). GSD1A is a rare genetic disorder that impairs the body's ability to break down glycogen into glucose, leading to a variety of symptoms including low blood sugar levels, growth retardation, and accumulation of glycogen in the liver and kidneys, potentially causing organ damage. This test is particularly important for individuals with a family history of GSD1A or those exhibiting symptoms suggestive of the disease. Early detection through genetic testing can facilitate prompt management and treatment strategies, significantly improving the quality of life and health outcomes for affected individuals. Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, the test involves collecting a DNA sample, usually through a blood draw or cheek swab. The sample is then analyzed for specific mutations in the G6PC gene that confirm the diagnosis of GSD1A. The cost of the test is 4400 AED, reflecting the specialized technology and expertise required to accurately identify the genetic mutations associated with the condition.
GAA Gene Glycogen storage disease type 2 Genetic Test Cost
Glycogen Storage Disease Type 2, also known as Pompe disease, is a rare genetic disorder caused by mutations in the GAA gene. This gene is responsible for producing an enzyme called acid alpha-glucosidase, which is crucial for breaking down glycogen into glucose within cells. Mutations in the GAA gene lead to the accumulation of glycogen in various tissues, particularly in muscles, impairing their function. To diagnose this condition, genetic testing for mutations in the GAA gene is essential. DNA Labs UAE offers a comprehensive genetic test to identify mutations in the GAA gene, aiding in the diagnosis of Glycogen Storage Disease Type 2. The test is a vital tool for confirming the disease, understanding its severity, and planning appropriate treatment and management strategies. The cost of the GAA gene genetic test at DNA Labs UAE is 4400 AED. The test involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed in the laboratory to detect the presence of mutations in the GAA gene. Results from this test can provide crucial information for affected individuals and their families regarding the condition, potential treatments, and the risk of passing the mutation to future generations.
