Search Results for: feed
PCCA Gene Propionic Acidemia Genetic Test Cost
The PCCA Gene Propionic Acidemia Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the PCCA gene, which are responsible for propionic acidemia. This rare genetic disorder disrupts the normal metabolism of certain parts of proteins and lipids, leading to the accumulation of propionic acid in the body. Symptoms can be severe and include poor feeding, vomiting, lethargy, and long-term health issues without prompt and proper treatment. The test is crucial for early detection, enabling targeted interventions and management strategies to mitigate the effects of the disorder. It involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed for specific genetic mutations in the PCCA gene. Priced at 4400 AED, the test is an investment in health, offering invaluable information for affected individuals and their families. Early diagnosis through the PCCA Gene Propionic Acidemia Genetic Test at DNA Labs UAE can significantly improve the quality of life and outcomes for those with propionic acidemia, making it a critical tool in the management of this rare condition.
NAGS Gene N-Acetylglutamate Synthase Deficiency Genetic Test Cost
The NAGS Gene N-Acetylglutamate Synthase Deficiency Genetic Test is a specialized diagnostic tool used to identify mutations in the NAGS gene, which are associated with N-Acetylglutamate Synthase (NAGS) deficiency. NAGS deficiency is a rare inherited disorder that disrupts the urea cycle, leading to an accumulation of ammonia in the blood, which can cause serious health issues, including neurological damage and, in severe cases, death if not treated promptly. Early diagnosis through genetic testing is crucial for the management and treatment of this condition. The test involves analyzing the patient's DNA to detect mutations in the NAGS gene that would indicate NAGS deficiency. It is a critical step for families with a history of the condition or for individuals presenting symptoms related to urea cycle disorders. Conducted by DNA Labs UAE, a leading provider of genetic testing services in the region, the NAGS Gene N-Acetylglutamate Synthase Deficiency Genetic Test is priced at 4400 AED. DNA Labs UAE employs state-of-the-art technology and adheres to stringent quality controls to ensure accurate and reliable test results, providing essential information for the effective management of the condition.
MMACHC Gene Methylmalonic Aciduria CblC Type Genetic Test Cost
The MMACHC gene methylmalonic aciduria (cobalamin deficiency) cblC type genetic test is a specialized diagnostic tool used to identify mutations in the MMACHC gene, which are responsible for causing methylmalonic aciduria cblC type. This condition is an inherited metabolic disorder characterized by the body's inability to process certain fats and proteins properly, leading to a buildup of toxic substances like methylmalonic acid in the body. Symptoms can include developmental delay, feeding difficulties, lethargy, and failure to thrive, among others. Early detection through genetic testing can be crucial in managing symptoms and preventing serious complications. The test is conducted at DNA Labs UAE, a leading facility in genetic testing and analysis. The cost of the test is 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify mutations in the MMACHC gene. By opting for this test at DNA Labs UAE, patients can expect comprehensive support, from initial consultation through to result interpretation and advice on management or treatment options. This test is a vital resource for families with a history of the condition or for individuals showing symptoms of methylmalonic aciduria cblC type, offering a pathway to better understanding and managing this genetic disorder.
BCKDHA Gene Maple Syrup Urine Disease Type 1a Genetic Test Cost
The BCKDHA Gene Maple Syrup Urine Disease Type 1a Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to detect mutations in the BCKDHA gene. These mutations are responsible for the most common form of Maple Syrup Urine Disease (MSUD), Type 1a. MSUD is a rare inherited metabolic disorder characterized by the body's inability to process certain amino acids properly, leading to a buildup of toxic substances that can cause severe neurological damage if not treated early. The test is particularly crucial for early diagnosis and management of the condition, which can significantly improve the quality of life and prognosis for affected individuals. Conducted through a simple blood sample, the genetic test searches for specific mutations in the BCKDHA gene that indicate the presence of MSUD Type 1a. Priced at 4400 AED, the test is an investment in health, especially for families with a history of the disorder or those who have had children with unexplained symptoms related to the disease. DNA Labs UAE provides this testing service with high accuracy and confidentiality, ensuring that individuals and families receive the necessary information for informed healthcare decisions.
BCKDHB Gene Maple Syrup Urine Disease Type 1b Genetic Test Cost
The BCKDHB gene maple syrup urine disease type 1b genetic test is a specialized diagnostic procedure aimed at identifying mutations in the BCKDHB gene, which are responsible for causing maple syrup urine disease (MSUD) type 1b. MSUD is a rare inherited metabolic disorder characterized by the body's inability to properly process certain amino acids, leading to a distinctive sweet-smelling urine, similar to maple syrup, along with potentially severe neurological complications if left untreated. This genetic test is crucial for early detection and management of the condition, allowing for tailored dietary and medical interventions that can significantly improve outcomes and quality of life for affected individuals. Conducted by DNA Labs UAE, a leading facility in genetic diagnostics, the test provides a comprehensive analysis of the BCKDHB gene to identify disease-causing mutations. The cost of the BCKDHB gene maple syrup urine disease type 1b genetic test is 4400 AED. While the price may seem high, the test's value in facilitating early and accurate diagnosis cannot be overstated, potentially preventing life-threatening complications and enabling affected individuals to lead healthier lives.
KCNJ11 Gene Hyperinsulinemic Hypoglycemia Type 2 Genetic Test Cost
The KCNJ11 gene plays a crucial role in regulating insulin release from the pancreas. Mutations in this gene can lead to a condition known as Hyperinsulinemic Hypoglycemia Type 2, characterized by excessive insulin production leading to low blood sugar levels. This condition, often detected in infancy or early childhood, can cause symptoms ranging from mild hypoglycemia to severe, life-threatening episodes. To diagnose this genetic condition, the KCNJ11 Gene Hyperinsulinemic Hypoglycemia Type 2 Genetic Test is employed. This specialized test is designed to identify mutations in the KCNJ11 gene that are responsible for the disorder. Early detection through genetic testing is crucial for managing symptoms, preventing complications, and guiding treatment decisions. The test is available at DNA Labs UAE, a reputable facility known for its advanced genetic testing services. The cost of the test is 3200 AED, an investment that provides invaluable information for affected individuals and their families. By confirming a diagnosis, the test enables tailored treatment plans that can significantly improve the quality of life for those with Hyperinsulinemic Hypoglycemia Type 2.
ASS1 Gene Citrullinemia Genetic Test Cost
The ASS1 Gene Citrullinemia Genetic Test is a specialized diagnostic procedure aimed at identifying mutations in the ASS1 gene, which is pivotal for diagnosing Citrullinemia, a rare genetic disorder. Citrullinemia results from the body's inability to eliminate ammonia from the bloodstream due to a deficiency in the enzyme argininosuccinate synthetase, which is crucial for the urea cycle. This condition can lead to harmful levels of ammonia in the blood, causing severe implications for an individual's health, including neurological impairments and, if untreated, can be life-threatening. Conducted at DNA Labs UAE, a leading facility in genetic testing, the test involves collecting a DNA sample, typically through a blood draw or a cheek swab, to analyze the genetic makeup of the ASS1 gene. This comprehensive analysis helps in identifying any mutations that may lead to the dysfunction of the enzyme responsible for ammonia detoxification in the liver. The cost of the ASS1 Gene Citrullinemia Genetic Test at DNA Labs UAE is set at 4400 AED. This price reflects the sophisticated technology and expertise required to accurately diagnose this condition, ensuring that individuals receive the necessary information for proper management and treatment. Early detection through this genetic test can significantly improve the quality of life for those affected by Citrullinemia by allowing for timely interventions and personalized treatment plans.
CPT2 Gene Carnitine palmitoyltransferase 2 deficiency lethal neonatal Genetic Test Cost
The CPT2 gene is responsible for the production of the Carnitine Palmitoyltransferase II enzyme, which plays a critical role in the body's ability to convert fats into energy, particularly during periods of fasting. A deficiency in this enzyme due to mutations in the CPT2 gene can lead to a condition known as Carnitine Palmitoyltransferase II deficiency. This metabolic disorder can manifest in various forms, with the lethal neonatal form being the most severe. Affected infants experience significant health issues soon after birth, including liver dysfunction, cardiovascular problems, and muscle weakness, often leading to fatal outcomes if not promptly diagnosed and treated. To diagnose this genetic condition, DNA Labs UAE offers a specialized genetic test targeting the CPT2 gene to identify mutations that may lead to Carnitine Palmitoyltransferase II deficiency. The test is crucial for early detection, especially in the neonatal period, allowing for timely intervention and management strategies to be implemented. This test is priced at 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify and interpret genetic mutations associated with this condition. Conducted in a state-of-the-art laboratory setting by qualified geneticists, this test represents a vital tool in the battle against lethal neonatal Carnitine Palmitoyltransferase II deficiency, offering hope for affected families through early diagnosis and the potential for targeted treatment strategies.