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SLC26A6 Gene Hyperoxaluria SLC26A6 Related Genetic Test Cost
The SLC26A6 gene plays a crucial role in the regulation of oxalate and chloride ions in the body, impacting the renal handling of oxalate and contributing to the balance of oxalate levels. Mutations or dysfunction in the SLC26A6 gene can lead to hyperoxaluria, a condition characterized by an excessive urinary excretion of oxalate, which can result in kidney stones and, in severe cases, kidney damage. Hyperoxaluria related to the SLC26A6 gene can be either primary, due to genetic factors, or secondary, resulting from dietary factors, other diseases, or additional genetic conditions. To diagnose and manage this condition effectively, genetic testing for mutations in the SLC26A6 gene is available. In the United Arab Emirates, DNA Labs UAE offers a specific genetic test to identify alterations in the SLC26A6 gene that may contribute to hyperoxaluria. This test is crucial for individuals with a clinical history suggestive of hyperoxaluria or a family history of kidney stones or kidney disease, as it can confirm the genetic basis of the condition, guide treatment decisions, and inform family planning. The cost of the SLC26A6 related genetic test at DNA Labs UAE is 4400 AED. This investment in genetic testing can provide valuable insights into the genetic underpinnings of hyperoxaluria, facilitating personalized treatment approaches and preventive measures to mitigate the risk of kidney stones and potential kidney damage associated with the condition.
PCBD1 Gene Hyperphenylalaninemia BH4 Deficient Type D Genetic Test Cost
The PCBD1 Gene Hyperphenylalaninemia BH4 Deficient Type D Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the PCBD1 gene. These mutations are associated with Hyperphenylalaninemia BH4 Deficient Type D, a rare metabolic disorder. This condition affects the body's ability to process the amino acid phenylalanine, leading to its accumulation which can cause various neurological issues if left untreated. The test, priced at 4400 AED, offers a critical insight for early diagnosis and management, enabling tailored treatment plans to prevent potential complications. DNA Labs UAE, with its state-of-the-art facilities, provides accurate and reliable results for this essential genetic test.
PTS Gene Hyperphenylalaninemia BH4-Deficient Type A Genetic Test Cost
The PTS Gene Hyperphenylalaninemia BH4-Deficient Type A Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the PTS gene. This gene is crucial for the production of tetrahydrobiopterin (BH4), a coenzyme involved in the metabolism of several amino acids, including phenylalanine. Mutations in the PTS gene can lead to BH4-deficient hyperphenylalaninemia Type A, a rare metabolic disorder characterized by elevated levels of phenylalanine in the blood. This condition can lead to various neurological issues if left untreated. The test, priced at 4400 AED, is a critical tool for early detection and management, allowing for appropriate treatment plans to be devised to mitigate the risk of severe complications associated with this genetic disorder. DNA Labs UAE utilizes advanced genetic testing technologies to ensure accurate and reliable results, facilitating the best possible outcomes for affected individuals and their families.
PRODH Gene Hyperprolinemia Type 1 Genetic Test Cost
The PRODH Gene Hyperprolinemia Type 1 Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, designed to detect mutations in the PRODH gene, which are responsible for Hyperprolinemia Type 1. This condition is a rare metabolic disorder characterized by elevated levels of the amino acid proline in the blood, potentially leading to various neurological and psychiatric manifestations, including seizures, intellectual disability, and schizophrenia. The test involves analyzing the patient's DNA to identify any genetic anomalies within the PRODH gene that could lead to the disorder. With a cost of 4400 AED, the test is a crucial step towards accurate diagnosis, allowing for appropriate management and treatment plans tailored to the patient's specific genetic makeup. Conducted in the state-of-the-art facilities of DNA Labs UAE, this genetic test represents a significant advancement in the field of personalized medicine and genetic disorders diagnosis.
ALDH4A1 Gene Hyperprolinemia Type 2 Genetic Test Cost
The ALDH4A1 Gene Hyperprolinemia Type 2 Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to detect mutations in the ALDH4A1 gene. These mutations are associated with Hyperprolinemia Type 2, a rare inherited disorder that affects the body's ability to break down the amino acid proline, leading to its accumulation. This can result in various neurological and physical symptoms, making early detection crucial for management and treatment. The test involves analyzing the patient's DNA to identify any genetic variations in the ALDH4A1 gene that could lead to the condition. It's a critical tool for individuals with a family history of Hyperprolinemia Type 2 or those exhibiting symptoms related to proline accumulation. Priced at 4400 AED, this genetic test is conducted at DNA Labs UAE, a facility known for its advanced genetic testing services and commitment to providing accurate, confidential results. The test offers valuable insights for affected individuals and their families, enabling informed decisions about health and treatment options.
SARS2 Gene Hyperuricemia Pulmonary Hypertension Renal Failure and Alkalosis Genetic Test Cost
The "SARS2 Gene Hyperuricemia Pulmonary Hypertension Renal Failure and Alkalosis Genetic Test" is a specialized diagnostic tool available at DNA Labs UAE, designed to identify genetic mutations associated with a complex spectrum of conditions. These conditions include hyperuricemia, which is an excess of uric acid in the blood; pulmonary hypertension, a type of high blood pressure that affects the arteries in the lungs and the right side of the heart; renal failure, which is a decrease in kidney function; and alkalosis, a condition where the body fluids have excess base (alkali). The test specifically looks for mutations in the SARS2 gene, which could indicate a predisposition to developing these health issues. The cost of the test is 4400 AED, and it involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed in the laboratory. This genetic testing can be crucial for early diagnosis, allowing for timely intervention and management of these conditions. It can also provide valuable information for family planning and the assessment of risk for family members. Conducted in the state-of-the-art facilities of DNA Labs UAE, this test represents a significant advancement in personalized medicine and genetic understanding of complex diseases.
CYP11B2 Gene Hypoaldosteronism Congenital Due to CMO I Deficiency Genetic Test Cost
The CYP11B2 gene plays a crucial role in the production of aldosterone, a hormone vital for regulating blood pressure and electrolyte balance. Hypoaldosteronism congenital due to CMO I (Corticosterone Methyloxidase I) deficiency is a rare genetic disorder affecting aldosterone synthesis, leading to symptoms such as salt loss, dehydration, and failure to thrive in infants. The condition results from mutations in the CYP11B2 gene, which encodes an enzyme essential for the final steps of aldosterone production. To diagnose this condition, a genetic test targeting the CYP11B2 gene can be performed. This test is available at DNA Labs UAE, a facility equipped with advanced genetic testing technologies. The test cost is 4400 AED and is designed to identify mutations in the CYP11B2 gene that lead to CMO I deficiency and consequently hypoaldosteronism. Early diagnosis through this genetic test can facilitate timely management and treatment of the condition, significantly improving the patient's quality of life.
APOA1 Gene Hypoalphalipoproteinemia Genetic Test Cost
The APOA1 gene hypoalphalipoproteinemia genetic test is a specialized diagnostic tool designed to identify mutations in the APOA1 gene, which can lead to hypoalphalipoproteinemia. This condition is characterized by abnormally low levels of high-density lipoprotein (HDL) cholesterol in the blood, often referred to as "good" cholesterol. HDL plays a critical role in removing excess cholesterol from the bloodstream and transporting it to the liver for removal, hence, a deficiency can increase the risk of cardiovascular diseases. The test involves collecting a DNA sample, usually through a blood draw or a cheek swab, which is then analyzed in a laboratory to detect any genetic abnormalities in the APOA1 gene. This genetic testing is crucial for individuals with a family history of hypoalphalipoproteinemia or premature cardiovascular disease, as it can help in the early detection and management of the condition. In the UAE, this specific genetic test is available at DNA Labs, a reputable facility known for its comprehensive range of genetic testing services. The cost of the APOA1 gene hypoalphalipoproteinemia genetic test at DNA Labs UAE is 4400 AED. Given the implications of the test results for managing and potentially preventing cardiovascular diseases, it represents a significant investment in one's health. Early diagnosis and intervention can lead to lifestyle adjustments and treatments that may mitigate the risks associated with hypoalphalipoproteinemia.
