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SLC2A5 Gene Fructose uptake deficiency SLC2A5 related Genetic Test Cost
The SLC2A5 gene is responsible for encoding a protein that facilitates the transport of fructose, a type of sugar, into the cells of the body. Mutations in the SLC2A5 gene can lead to fructose uptake deficiency, a condition that affects the body's ability to properly metabolize fructose. This can result in various health issues, including gastrointestinal distress and potentially more severe metabolic complications. To diagnose this condition, a specific genetic test related to the SLC2A5 gene can be conducted. This test aims to identify mutations in the SLC2A5 gene that are indicative of fructose uptake deficiency. DNA Labs UAE offers this specialized genetic testing service. The cost of the SLC2A5-related genetic test at DNA Labs UAE is 4400 AED. This test is crucial for individuals experiencing symptoms related to fructose malabsorption or those with a family history of fructose uptake issues, as it can provide a definitive diagnosis and guide dietary and lifestyle adjustments to manage the condition effectively.
FBP1 Gene Fructose-16-bisphosphatase deficiency Genetic Test Cost
The FBP1 gene encodes the enzyme fructose-1,6-bisphosphatase, which plays a crucial role in the process of gluconeogenesis, the metabolic pathway that generates glucose from non-carbohydrate substrates. Mutations in the FBP1 gene can lead to a rare inherited metabolic disorder known as fructose-1,6-bisphosphatase deficiency. This condition is characterized by impaired glucose production, leading to symptoms such as hypoglycemia, particularly during fasting or infections, ketosis, and lactic acidosis. Early diagnosis and management are essential to prevent potentially severe outcomes. The genetic test for FBP1 gene fructose-1,6-bisphosphatase deficiency is a specialized diagnostic tool designed to detect mutations in the FBP1 gene that are responsible for the condition. This test is crucial for confirming the diagnosis, enabling appropriate management, and providing information for family planning. In the UAE, this genetic test is available at DNA Labs UAE, a leading facility in genetic diagnostics and personalized medicine. The cost of the test is 4400 AED. The process involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory to identify any mutations in the FBP1 gene. The results from this test can help guide treatment strategies, dietary recommendations, and inform family members about their risk of passing the condition onto future generations.
KHK Gene Fructosuria essential Genetic Test Cost
The "KHK Gene Fructosuria Essential Genetic Test" is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the KHK gene, which can lead to essential fructosuria. This condition is a rare, inherited metabolic disorder characterized by the inability to properly metabolize fructose, a type of sugar found in fruits, honey, and some sweeteners. Individuals with essential fructosuria typically exhibit elevated levels of fructose in their urine, although the condition is often benign and asymptomatic. The test is particularly important for individuals with a family history of metabolic disorders or for those exhibiting symptoms related to fructose metabolism issues. It involves collecting a DNA sample, usually through a blood draw or a cheek swab, which is then analyzed in the laboratory for the presence of specific mutations in the KHK gene that are known to cause essential fructosuria. At a cost of 4400 AED, the KHK Gene Fructosuria Essential Genetic Test is an investment in personal health, offering crucial insights for affected individuals or those at risk. Understanding one's genetic predisposition to essential fructosuria can help in making informed dietary choices and in the management of this condition, even though it is generally considered to have a benign prognosis. DNA Labs UAE, with its state-of-the-art facilities and expert team, ensures accurate and reliable test results, providing a solid foundation for personalized health management strategies.
FUCA1 Gene Fucosidosis Genetic Test Cost
The FUCA1 gene fucosidosis genetic test is a specialized diagnostic tool used to identify mutations in the FUCA1 gene, which are responsible for the rare lysosomal storage disorder known as fucosidosis. This condition is characterized by a deficiency of the enzyme alpha-L-fucosidase, leading to the accumulation of fucose-containing glycolipids and glycoproteins in various tissues. Symptoms can include neurological impairment, growth retardation, and skin lesions, among others. The test involves analyzing DNA to detect mutations in the FUCA1 gene, offering crucial information for the diagnosis, management, and genetic counseling of affected individuals and their families. Conducted at DNA Labs UAE, a leading facility in genetic testing, the test ensures accuracy and confidentiality in the results. The cost of the FUCA1 gene fucosidosis genetic test is 4400 AED. This price reflects the comprehensive analysis and the sophisticated technology used in identifying the genetic mutations associated with the condition. Given the rarity of fucosidosis and the specialized nature of this test, it represents a valuable investment in the health and well-being of patients suspected of having this genetic disorder.
FH Gene Fumarase deficiency Genetic Test Cost
The FH Gene Fumarase Deficiency Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, aimed at detecting mutations in the FH gene, which are responsible for fumarase deficiency. Fumarase deficiency is a rare metabolic disorder that can lead to a wide range of symptoms, including severe neurological impairment and physical developmental delays. The test involves analyzing the individual's DNA to identify any genetic abnormalities in the FH gene, which plays a crucial role in the mitochondrial Krebs cycle for energy production. With a test cost of 4400 AED, DNA Labs UAE provides a comprehensive analysis to help in the early detection and management of this condition. Early diagnosis through the FH Gene Fumarase Deficiency Genetic Test can be pivotal in managing symptoms, preventing complications, and improving the quality of life for individuals affected by this disorder. DNA Labs UAE utilizes advanced genetic testing techniques to ensure accurate and reliable results, making it an essential resource for individuals with a family history of fumarase deficiency or those exhibiting symptoms associated with the condition.
ABAT Gene GABA-transaminase deficiency Genetic Test Cost
The ABAT Gene GABA-transaminase deficiency genetic test is a specialized diagnostic tool designed to identify mutations in the ABAT gene, which are associated with GABA-transaminase deficiency. This rare genetic disorder impacts the enzyme responsible for the degradation of gamma-aminobutyric acid (GABA), leading to an accumulation of GABA and subsequent neurological issues. Symptoms can include seizures, developmental delays, and a range of neuropsychiatric manifestations. The test is performed by analyzing a patient's DNA sample, usually obtained through a blood draw, to look for mutations in the ABAT gene that indicate the presence of GABA-transaminase deficiency. This precise genetic testing is crucial for confirming the diagnosis, which can then guide treatment strategies and management plans tailored to the individual's needs. DNA Labs UAE offers this comprehensive genetic test at a cost of 4400 AED. By providing this service, DNA Labs UAE aims to facilitate early and accurate diagnosis, enabling affected individuals and their families to understand their condition better and seek appropriate care and interventions. The test represents an important step in the journey towards personalized medicine, where treatments and management strategies are increasingly based on the individual's genetic makeup.
GALK1 Gene Galactokinase deficiency Genetic Test Cost
The GALK1 gene is responsible for producing the enzyme galactokinase, which plays a crucial role in the metabolism of galactose, a type of sugar found in milk and other dairy products. Mutations in the GALK1 gene can lead to galactokinase deficiency, a rare genetic disorder that prevents the body from properly processing galactose. This condition can lead to various health issues, including cataracts, delayed growth, and learning difficulties if not managed properly. To diagnose this condition, a genetic test can be conducted to identify mutations in the GALK1 gene. DNA Labs UAE offers a comprehensive genetic test for galactokinase deficiency, providing a reliable means of diagnosis for those suspected of having the condition or carriers of the gene mutation. The test is priced at 3200 AED and involves analyzing the patient's DNA to detect any abnormalities in the GALK1 gene that could lead to the disorder. By opting for this test, individuals can gain crucial insights into their genetic health, enabling them to make informed decisions regarding their dietary intake and management of the condition.
GALE Gene Galactose epimerase deficiency Genetic Test Cost
The GALE Gene Galactose Epimerase Deficiency Genetic Test is a specialized diagnostic tool used to detect mutations in the GALE gene, which can lead to Galactose Epimerase Deficiency. This condition is a rare genetic disorder that affects the body's ability to process galactose, a sugar found in milk and other dairy products, leading to a range of metabolic issues. The test involves analyzing the patient's DNA to identify any genetic alterations in the GALE gene that could disrupt the normal metabolism of galactose. Performed at DNA Labs UAE, a leading facility in genetic testing, this test offers a critical resource for early diagnosis and management of Galactose Epimerase Deficiency. By identifying the condition early, healthcare providers can tailor dietary and medical interventions to prevent the serious health complications associated with the disorder. The cost of the GALE Gene Galactose Epimerase Deficiency Genetic Test is 4400 AED. While the price may seem significant, the test provides invaluable information for affected individuals and their families, enabling them to make informed decisions about health and treatment options.
