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GCK Gene Hyperinsulinemic Hypoglycemia Type 3 Genetic Test Cost
The "GCK Gene Hyperinsulinemic Hypoglycemia Type 3 Genetic Test" is a specialized diagnostic procedure designed to identify mutations in the GCK gene, which are associated with Hyperinsulinemic Hypoglycemia Type 3 (HH Type 3). HH Type 3 is a genetic disorder characterized by the excessive production of insulin, leading to recurrent episodes of low blood sugar (hypoglycemia). The GCK gene plays a crucial role in glucose metabolism, and mutations in this gene can disrupt normal insulin secretion, causing the hypoglycemic episodes observed in affected individuals. This genetic test is a critical tool for confirming the diagnosis of HH Type 3, enabling healthcare providers to tailor treatment plans to manage symptoms effectively and prevent potential complications associated with the condition. Early diagnosis and intervention are key to improving the quality of life for individuals with HH Type 3. The test is available at DNA Labs UAE, a reputable facility known for its advanced genetic testing services. The cost of the test is 4400 AED, reflecting the intricate technologies and expertise required to accurately identify mutations in the GCK gene. By opting for this test at DNA Labs UAE, patients and their families can expect reliable results, comprehensive support, and guidance on managing the condition from a team of genetic specialists.
SLC16A1 Gene Hyperinsulinemic Hypoglycemia Type 7 Genetic Test Cost
The SLC16A1 gene hyperinsulinemic hypoglycemia type 7 genetic test is a specialized diagnostic examination designed to identify mutations in the SLC16A1 gene, which are linked to a rare form of congenital hyperinsulinemic hypoglycemia. This condition is characterized by excessive insulin production leading to dangerously low blood sugar levels. The test is crucial for the early detection and management of this disorder, enabling healthcare providers to tailor appropriate treatment plans for affected individuals. Performed at DNA Labs UAE, a leading facility in genetic diagnostics, this test involves collecting a DNA sample, typically through a blood draw, from the patient. The sample is then analyzed using advanced genetic sequencing technologies to detect any abnormalities in the SLC16A1 gene that may be responsible for the condition. The cost of the SLC16A1 gene hyperinsulinemic hypoglycemia type 7 genetic test at DNA Labs UAE is set at 4400 AED. This price reflects the sophisticated nature of the testing process and the specialized expertise required to accurately interpret the results. For families and individuals facing the possibility of this rare genetic disorder, this test represents a critical step towards understanding and managing the condition effectively.
UCP2 Gene Hyperinsulinism UCP2 Related Genetic Test Cost
The UCP2 Gene Hyperinsulinism test, available at DNA Labs UAE for a cost of 4400 AED, is a specialized genetic test designed to detect mutations in the UCP2 gene, which have been associated with hyperinsulinism. Hyperinsulinism is a condition characterized by the excessive production of insulin by the pancreas, leading to low blood sugar levels (hypoglycemia). The UCP2 gene plays a crucial role in regulating the secretion of insulin and energy metabolism within the body's cells. This test is particularly important for individuals who may have a family history of hyperinsulinism or who exhibit symptoms of the condition, such as frequent episodes of hypoglycemia, seizures, and excessive hunger. By identifying specific genetic mutations in the UCP2 gene, healthcare providers can offer a more accurate diagnosis, tailor treatment plans to manage symptoms effectively, and provide genetic counseling to affected families. Conducted in the state-of-the-art facilities of DNA Labs UAE, the test involves collecting a small sample of the patient's blood or saliva. The sample is then analyzed using advanced genetic sequencing techniques to identify any mutations in the UCP2 gene. Results from this test can provide valuable insights into the genetic basis of hyperinsulinism and contribute to the development of personalized medicine approaches for managing the condition.
USF1 Gene Hyperlipidemia Familial Combined Susceptibility to Genetic Test Cost
The USF1 Gene Hyperlipidemia Familial Combined Susceptibility Genetic Test is a specialized diagnostic tool designed to identify individuals at risk for Familial Combined Hyperlipidemia (FCHL), a genetic disorder characterized by elevated levels of cholesterol and triglycerides in the blood. This condition is significant due to its association with an increased risk of cardiovascular diseases. The test specifically targets the USF1 gene, which has been implicated in the susceptibility to FCHL, making it a critical marker for assessing the risk of developing this condition. Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, the test involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed for specific mutations or variations in the USF1 gene that are known to contribute to FCHL. The results can provide valuable information for individuals with a family history of hyperlipidemia or early-onset heart disease, enabling them to take preventive measures or seek early treatment. The cost of the USF1 Gene Hyperlipidemia Familial Combined Susceptibility Genetic Test at DNA Labs UAE is 4400 AED. While the price may seem steep, the insights gained from this test can be invaluable in managing one's health and taking proactive steps towards preventing the development of serious cardiovascular conditions associated with Familial Combined Hyperlipidemia.
LPL Gene Hyperlipoproteinemia Type 1 Genetic Test Cost
The LPL Gene Hyperlipoproteinemia Type 1 Genetic Test is a specialized diagnostic procedure offered at DNA Labs UAE, designed to identify mutations in the LPL gene, which can lead to Type 1 hyperlipoproteinemia. This condition, also known as familial lipoprotein lipase deficiency, is a rare genetic disorder characterized by the inability to properly break down fats, leading to an accumulation of chylomicrons and triglycerides in the blood, and potentially resulting in pancreatitis, abdominal pain, and other complications. The test is crucial for individuals with a family history of hyperlipoproteinemia or those who have symptoms of the disorder, as it helps in confirming the diagnosis, enabling personalized treatment plans, and informing family planning decisions. Conducted through a simple blood sample, the genetic analysis focuses on detecting specific mutations within the LPL gene that are responsible for the condition. At DNA Labs UAE, the LPL Gene Hyperlipoproteinemia Type 1 Genetic Test is priced at 4400 AED. This cost reflects the comprehensive nature of the testing process, from the initial sample collection to the detailed genetic analysis and the provision of a conclusive report by the lab's expert geneticists. The test is an invaluable tool for affected individuals and their families to understand their genetic health, manage the condition effectively, and make informed healthcare decisions.
AASS Gene Hyperlysinemia Type 1 Genetic Test Cost
The AASS Gene Hyperlysinemia Type 1 Genetic Test is a specialized diagnostic tool used to detect mutations in the AASS gene, which are responsible for Hyperlysinemia Type 1, a rare metabolic disorder. This condition is characterized by an excess of the amino acid lysine in the blood, which can lead to various health issues, including developmental delays, seizures, and behavioral problems. The test is crucial for early detection and management of the condition, allowing for appropriate interventions and lifestyle adjustments to mitigate symptoms and improve quality of life. 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, which is then analyzed for specific genetic mutations in the AASS gene. The cost of the test is 4400 AED, reflecting the comprehensive analysis and detailed reporting provided by the lab. By identifying individuals with Hyperlysinemia Type 1, this genetic test plays a vital role in personalized medicine, offering affected families the information needed to make informed health and reproductive decisions.
ADK Gene Hypermethioninemia Due to Adenosine Kinase Deficiency Genetic Test Cost
**ADK Gene Hypermethioninemia Due to Adenosine Kinase Deficiency Genetic Test** This specialized genetic test is designed to diagnose hypermethioninemia caused by adenosine kinase (ADK) deficiency. Hypermethioninemia is a metabolic condition characterized by elevated levels of methionine in the blood, which can lead to various health issues if left untreated. The condition is attributed to mutations in the ADK gene, which plays a crucial role in the metabolism of adenosine, affecting methionine levels. Early detection through genetic testing is essential for managing the condition effectively. The test is offered at DNA Labs UAE, a leading facility equipped with advanced genetic testing technology. The process involves analyzing the patient's DNA to identify mutations in the ADK gene that are responsible for the condition. This targeted approach allows for a precise diagnosis, enabling healthcare providers to tailor treatment plans to the individual's specific needs. The cost of the test is 4400 AED, reflecting the comprehensive analysis and detailed insights it provides. This investment can be crucial for individuals at risk of or suspected to have hypermethioninemia due to ADK deficiency, as it opens the door to informed healthcare decisions and personalized management strategies. For those considering this test, it's advisable to consult with a healthcare professional or genetic counselor to understand its implications fully and how the results may impact treatment and lifestyle choices. DNA Labs UAE also offers support and guidance throughout the testing process, ensuring that patients and their families are well-informed and supported every step of the way.
SLC25A15 Gene Hyperornithinemia- Hyperammonemia – Homocitrullinuria Syndrome Genetic Test Cost
The SLC25A15 Gene Hyperornithinemia-Hyperammonemia-Homocitrullinuria (HHH) Syndrome Genetic Test is a specialized diagnostic examination offered at DNA Labs UAE. Priced at 4400 AED, this test targets the identification of mutations in the SLC25A15 gene, which are responsible for the rare metabolic disorder known as HHH syndrome. This condition is characterized by elevated levels of ornithine and ammonia in the blood, along with the presence of homocitrulline in urine, leading to various neurological, cognitive, and physical symptoms. The test involves collecting a DNA sample from the patient, which is then analyzed for specific genetic alterations associated with the syndrome. Early detection through this genetic testing is crucial for managing symptoms and preventing potential complications associated with HHH syndrome, providing a pathway for targeted treatment and genetic counseling for affected families.
