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SLC2A9 Gene Hypouricemia Renal Type 2 Genetic Test Cost
The SLC2A9 Gene Hypouricemia Renal Type 2 Genetic Test is a specialized diagnostic procedure offered at DNA Labs UAE, designed to identify mutations in the SLC2A9 gene. These mutations are associated with renal hypouricemia type 2, a rare genetic disorder characterized by abnormally low levels of uric acid in the blood due to impaired renal urate reabsorption. The condition can lead to various complications, including kidney stones and exercise-induced acute kidney injury. This genetic test is crucial for individuals with a clinical history suggestive of renal hypouricemia or those with a family history of the condition, as it provides definitive confirmation of the diagnosis. The test involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed for specific mutations in the SLC2A9 gene. Offered at a cost of 4400 AED, the test at DNA Labs UAE employs advanced genetic sequencing technologies to ensure accurate and reliable results. Understanding one's genetic status regarding the SLC2A9 gene can be vital for making informed decisions about treatment and management options, as well as for genetic counseling purposes.
ACAD8 Gene Isobutyryl-CoA Dehydrogenase Deficiency Genetic Test Cost
The ACAD8 gene is associated with the production of isobutyryl-CoA dehydrogenase, an enzyme crucial for breaking down certain fats in the body. A deficiency in this enzyme, due to mutations in the ACAD8 gene, can lead to a rare metabolic disorder known as Isobutyryl-CoA Dehydrogenase (IBD) deficiency. This condition can present a variety of symptoms, ranging from mild to severe, including developmental delays, muscle weakness, and metabolic crises. To diagnose this condition, a genetic test targeting the ACAD8 gene can be conducted. This test is designed to identify mutations in the ACAD8 gene that lead to IBD deficiency. It is a critical step in confirming the diagnosis, which can then guide treatment and management strategies for affected individuals. In the UAE, this specific genetic test is available at DNA Labs UAE, a leading facility in genetic diagnostics. The cost of the ACAD8 Gene Isobutyryl-CoA Dehydrogenase Deficiency Genetic Test is set at 4400 AED. This test is conducted with high precision and accuracy, offering vital information for patients and their families. Through this testing, individuals can gain a better understanding of their condition, enabling informed decisions about their health management and care.
IVD Gene Isovaleric Acidemia Genetic Test Cost
The IVD Gene Isovaleric Acidemia Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to detect mutations in the IVD gene, which are responsible for Isovaleric Acidemia (IVA). Isovaleric Acidemia is a rare genetic disorder characterized by the body's inability to properly break down a particular amino acid called leucine, leading to the accumulation of isovaleric acid in the blood, which can be toxic and cause serious health issues. Early detection through this genetic test allows for timely intervention and management of the condition, improving the quality of life for affected individuals. The test is priced at 3200 AED and involves analyzing the patient's DNA to look for specific mutations in the IVD gene. The process is conducted in the state-of-the-art facilities of DNA Labs UAE, ensuring high accuracy and reliability of the results. This test is particularly important for families with a history of Isovaleric Acidemia, as it can help in making informed decisions regarding family planning and in implementing dietary and medical interventions that can significantly reduce the impact of the disorder.
L2HGDH Gene L-2-Hydroxyglutaric Aciduria Genetic Test Cost
The L2HGDH gene L-2-hydroxyglutaric aciduria genetic test is a specialized diagnostic tool used to identify mutations in the L2HGDH gene, which are responsible for the rare metabolic disorder known as L-2-hydroxyglutaric aciduria. This condition is characterized by the accumulation of L-2-hydroxyglutaric acid in the body, leading to a range of neurological impairments and physical abnormalities. Symptoms can include developmental delay, seizures, and abnormalities in the cerebellum, affecting coordination and movement. The test involves analyzing the patient's DNA to detect mutations in the L2HGDH gene, providing crucial information for accurate diagnosis and management of the condition. Early detection through genetic testing can help in planning appropriate treatment strategies and interventions to manage symptoms and improve the quality of life for affected individuals. In the UAE, this genetic test is available at DNA Labs UAE, a leading provider of genetic testing services in the region. The cost of the L2HGDH gene L-2-hydroxyglutaric aciduria genetic test is 4400 AED. The test is conducted with high precision and accuracy, ensuring reliable results for patients and their families. By opting for this test at DNA Labs UAE, individuals suspected of having L-2-hydroxyglutaric aciduria can gain access to vital information that can guide their healthcare decisions and enable them to receive appropriate care and support.
LCT Gene Lactase Deficiency Congenital Genetic Test Cost
The LCT gene, responsible for the production of lactase, an enzyme crucial for the digestion of lactose in dairy products, can have variations leading to lactase deficiency. This condition, commonly known as lactose intolerance, can range from mild discomfort to severe digestive problems upon the consumption of lactose-containing foods. A congenital genetic test for lactase deficiency specifically examines mutations in the LCT gene to determine an individual's predisposition to this condition. At DNA Labs UAE, a state-of-the-art facility offering a comprehensive range of genetic testing services, individuals can undergo the LCT Gene Lactase Deficiency Congenital Genetic Test. This test is meticulously designed to identify mutations in the LCT gene, providing invaluable insights into one's genetic predisposition towards lactose intolerance. The test is priced at 4400 AED, reflecting the sophisticated technology and expertise involved in its execution. By opting for this test, individuals can gain a deeper understanding of their genetic makeup, empowering them with the knowledge to make informed dietary choices and manage potential symptoms of lactose intolerance more effectively.
AKT2 Gene Hypoinsulinemic Hypoglycemia with Hemihypertrophy Genetic Test Cost
The "AKT2 Gene Hypoinsulinemic Hypoglycemia with Hemihypertrophy Genetic Test" is a specialized diagnostic procedure aimed at identifying mutations in the AKT2 gene, which have been linked to a rare and complex condition characterized by low insulin levels leading to hypoglycemia, coupled with hemihypertrophy, a condition where one side of the body or a part of it grows more than the other. This genetic anomaly is pivotal in understanding the underlying causes of these symptoms and tailoring a precise treatment plan for affected individuals. Performed at DNA Labs UAE, a leading facility in genetic diagnostics, the test involves analyzing the patient's DNA to detect any abnormalities in the AKT2 gene that could explain the clinical manifestations of hypoinsulinemic hypoglycemia and hemihypertrophy. The process is comprehensive, employing the latest technologies in genetic sequencing to ensure accurate and reliable results. The cost of the test is set at 3200 AED, reflecting the intricate nature of the genetic analysis and the specialized expertise required to interpret the results. This investment is crucial for affected families seeking answers and guidance on managing this rare condition, potentially offering a clearer prognosis and informing decisions on personalized treatment strategies.
TRPM6 Gene Hypomagnesemia Type 1 Genetic Test Cost
The "TRPM6 Gene Hypomagnesemia Type 1 Genetic Test" is a specialized diagnostic procedure aimed at identifying mutations in the TRPM6 gene, which are known to cause Hypomagnesemia Type 1, a rare inherited condition characterized by low levels of magnesium in the blood. This condition can lead to various symptoms, including muscle spasms, seizures, and irregular heartbeats, making early diagnosis crucial for effective management and treatment. Performed at DNA Labs UAE, this test involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed to detect any genetic abnormalities in the TRPM6 gene. The process is highly sophisticated, requiring state-of-the-art technology and expertise in genetic analysis. The cost of the TRPM6 Gene Hypomagnesemia Type 1 Genetic Test at DNA Labs UAE is 4400 AED. While the price might seem high, it reflects the complexity of the testing process and the invaluable insights it provides into managing and treating Hypomagnesemia Type 1. Early detection through this test can significantly improve the quality of life for individuals with this condition by enabling tailored treatment strategies and preventive measures.
AGXT Gene Hyperoxaluria Type 1 Genetic Test Cost
The AGXT Gene Hyperoxaluria Type 1 Genetic Test is a specialized diagnostic procedure designed to identify mutations in the AGXT gene, which is responsible for Primary Hyperoxaluria Type 1 (PH1). PH1 is a rare genetic disorder characterized by the excessive production of oxalate, leading to kidney stones, nephrocalcinosis, and potentially kidney failure. This test is crucial for individuals with a family history of the condition or those exhibiting symptoms related to kidney stones and renal impairment. Performed at DNA Labs UAE, the test involves analyzing the patient's DNA to detect any genetic alterations in the AGXT gene that could result in the abnormal production of oxalate. The process is conducted with precision and confidentiality, ensuring accurate results that can guide clinical decisions, including personalized treatment plans and management strategies to prevent kidney damage. The cost of the AGXT Gene Hyperoxaluria Type 1 Genetic Test is 4400 AED. Although the price may seem significant, the value of early detection and the potential to mitigate the severe complications associated with PH1 cannot be understated. For those at risk, this test provides a critical pathway to proactive health management and improved quality of life.
