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SLC34A3 Gene Hypophosphatemic Rickets with Hypercalciuria Genetic Test Cost
The SLC34A3 gene hypophosphatemic rickets with hypercalciuria genetic test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the SLC34A3 gene. This gene plays a crucial role in phosphate homeostasis, and mutations can lead to a rare form of rickets characterized by low levels of phosphate in the blood (hypophosphatemia) alongside high levels of calcium in the urine (hypercalciuria). This condition not only affects bone mineralization but can also lead to bone pain, weakness, and skeletal deformities. The test, priced at 4400 AED, involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory to detect any genetic anomalies associated with the condition. By pinpointing specific genetic mutations, this test can confirm a diagnosis of hypophosphatemic rickets with hypercalciuria, thereby enabling healthcare providers to tailor treatment plans more effectively to manage symptoms and improve the patient's quality of life. This genetic testing is a critical step for families seeking answers to inherited conditions, providing them with crucial information for understanding the condition and making informed health and lifestyle decisions.
FGF23 Gene Hypophosphatemic Rickets Autosomal Dominant Genetic Test Cost
The FGF23 Gene Hypophosphatemic Rickets Autosomal Dominant Genetic Test is a specialized diagnostic procedure aimed at identifying mutations in the FGF23 gene, which are known to cause autosomal dominant hypophosphatemic rickets (ADHR). This condition is characterized by low phosphate levels in the blood due to impaired phosphate reabsorption in the kidneys, leading to bone softening and weakness, known as rickets in children and osteomalacia in adults. The FGF23 gene plays a crucial role in phosphate homeostasis, and mutations in this gene can disrupt this balance, causing the disease. This genetic test is conducted at DNA Labs UAE, a leading facility in genetic diagnostics and research. The test involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed in the lab for specific mutations in the FGF23 gene that are indicative of ADHR. The cost of the test is 4400 AED, reflecting the specialized nature of the analysis and the expertise required to interpret the results. By accurately identifying the genetic basis of hypophosphatemic rickets, this test enables targeted treatment approaches, such as phosphate supplements or calcitriol, and provides valuable information for family planning and genetic counseling. It represents a critical step in the diagnosis and management of individuals with this rare but impactful condition.
SLC22A12 Gene Hypouricemia Renal Type 1 Genetic Test Cost
The SLC22A12 gene hypouricemia renal type 1 genetic test is a specialized diagnostic procedure aimed at detecting mutations in the SLC22A12 gene, which can lead to renal hypouricemia type 1. This condition is characterized by abnormally low levels of uric acid in the blood, due to an impairment in the kidneys' ability to reabsorb uric acid from the urine. This can result in a variety of health issues, including an increased risk for kidney stones and kidney failure. The test is conducted at DNA Labs UAE, a reputable facility known for its advanced genetic testing services. By analyzing a sample of the patient's DNA, the test can identify specific mutations in the SLC22A12 gene that are responsible for the condition. This information is crucial for the accurate diagnosis and management of renal hypouricemia type 1, allowing for targeted treatment strategies and lifestyle adjustments to mitigate the risk of complications. The cost of the SLC22A12 gene hypouricemia renal type 1 genetic test at DNA Labs UAE is 4400 AED. This price reflects the sophisticated technology and expertise required to accurately identify mutations in the SLC22A12 gene. Patients considering this test are advised to consult with their healthcare provider to discuss its relevance and potential outcomes in the context of their individual health status and family history.
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.
IGF1R Gene Insulin-like Growth Factor Resistance Genetic Test Cost
The "IGF1R Gene Insulin-like Growth Factor Resistance Genetic Test" is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the IGF1R gene, which can lead to insulin-like growth factor resistance. This condition can impact growth and development, and it's essential for the diagnosis and management of related disorders. By analyzing the patient's DNA, the test seeks to uncover genetic variations that could affect the function of the insulin-like growth factor 1 receptor, which plays a crucial role in growth and development through its influence on cell growth, differentiation, and survival. The cost of the test is set at 4400 AED, offering a vital resource for individuals and healthcare providers looking to understand and address growth-related conditions at a molecular level. This test is a critical tool for personalized medicine, enabling targeted interventions and management strategies based on the patient's genetic makeup.
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.
GALC Gene Krabbe Disease Genetic Test Cost
The GALC Gene Krabbe Disease Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, aimed at detecting mutations in the GALC gene, which are responsible for Krabbe disease. Krabbe disease is a rare, inherited disorder that affects the nervous system, leading to severe physical and mental deterioration. Early detection through this genetic test is crucial for managing the disease's progression and exploring potential treatment options. The test involves collecting a DNA sample, typically through a blood draw or cheek swab, and analyzing it for specific genetic changes in the GALC gene. The cost of the GALC Gene Krabbe Disease Genetic Test at DNA Labs UAE is 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify the genetic markers associated with this condition.