Search Results for: results
AGA Gene Aspartylglucosaminuria Genetic Test Cost
The AGA Gene Aspartylglucosaminuria Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to detect mutations in the AGA gene. These mutations are responsible for aspartylglucosaminuria, a rare inherited lysosomal storage disorder. This condition affects the body's ability to break down certain glycoproteins, leading to their accumulation and causing progressive intellectual disability and physical deterioration over time. Early detection through genetic testing is crucial for managing symptoms and improving quality of life. The test is priced at 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify the genetic variations associated with the disorder. DNA Labs UAE offers this test as part of its comprehensive suite of genetic diagnostics, providing essential information for affected individuals and their families to make informed health decisions.
ST6GAL2 Gene Beta-Galactosamide alpha-26-Sialyltransferase 2 deficiency Genetic Test Cost
The ST6GAL2 gene plays a crucial role in the biosynthesis of the sialylated glycoproteins, which are important for various biological functions, including cell signaling and immune response. The Beta-Galactosamide alpha-2,6-Sialyltransferase 2, encoded by the ST6GAL2 gene, is an enzyme that adds sialic acid to the terminal positions of glycoproteins and glycolipids. Deficiency or dysfunction in this enzyme due to genetic variations can lead to a range of physiological and developmental issues. To diagnose conditions related to the ST6GAL2 gene deficiency, a specific genetic test is available. This test involves analyzing the DNA to identify mutations in the ST6GAL2 gene that could lead to enzyme deficiency. It's a critical tool for healthcare providers to diagnose potential genetic disorders related to this enzyme's malfunction, enabling them to devise appropriate treatment and management plans for affected individuals. The genetic test for ST6GAL2 gene Beta-Galactosamide alpha-2,6-Sialyltransferase 2 deficiency is offered by DNA Labs UAE, a leading provider of genetic testing services in the United Arab Emirates. The test is priced at 4400 AED, reflecting the specialized nature of the analysis and the advanced technology used to identify the genetic variations accurately. By opting for this test at DNA Labs UAE, patients and healthcare providers can expect reliable results that can significantly aid in the understanding and management of conditions associated with ST6GAL2 gene deficiency.
UPB1 Gene Beta-ureidopropionase deficiency Genetic Test Cost
The UPB1 gene beta-ureidopropionase deficiency genetic test is a diagnostic procedure offered by DNA Labs UAE, designed to detect mutations in the UPB1 gene that are responsible for beta-ureidopropionase deficiency. This rare genetic disorder affects the body's ability to properly break down certain proteins, leading to an accumulation of toxic substances that can cause neurological and developmental problems. The test, priced at 4400 AED, involves analyzing a DNA sample, typically obtained through a blood draw, to identify any genetic anomalies in the UPB1 gene. Early detection through this test can be crucial for managing symptoms and preventing complications associated with the condition. DNA Labs UAE provides this specialized testing service with the aim of supporting accurate diagnosis and facilitating appropriate treatment strategies for affected individuals.
HSD3B7 Gene Bile acid synthesis defect type 1 congenital Genetic Test Cost
The HSD3B7 gene is essential in the complex process of bile acid synthesis. Defects in this gene can lead to a rare disorder known as congenital bile acid synthesis defect type 1 (CBAS1). This condition disrupts the body's ability to properly produce bile acids, which are crucial for digestion and absorption of fats and fat-soluble vitamins. Symptoms can include jaundice, failure to thrive, and liver dysfunction, making early diagnosis and treatment vital. To diagnose this genetic condition, a specific genetic test targeting the HSD3B7 gene can be conducted. This test examines the DNA for mutations in the HSD3B7 gene that are known to cause CBAS1. It's a crucial step for confirming the diagnosis, enabling appropriate treatment plans, and providing information for family planning. In the UAE, DNA Labs offers this specialized genetic test. The cost of the HSD3B7 gene bile acid synthesis defect type 1 congenital genetic test is 4400 AED. Conducted in a state-of-the-art laboratory by experienced geneticists, the test provides accurate and reliable results, ensuring that affected individuals and their families receive the necessary support and information for managing this condition.
AKR1D1 Gene Bile acid synthesis defect type 2 congenital Genetic Test Cost
The AKR1D1 gene plays a crucial role in the process of bile acid synthesis, which is essential for the digestion and absorption of fats and fat-soluble vitamins in the intestines. A defect in this gene can lead to a rare disorder known as Bile Acid Synthesis Defect Type 2, a congenital condition that can cause serious liver and growth problems in affected individuals from an early age. To diagnose this condition, genetic testing is vital. DNA Labs UAE offers a specific genetic test aimed at identifying mutations in the AKR1D1 gene that are responsible for Bile Acid Synthesis Defect Type 2. This test is a crucial step in confirming the diagnosis, which can then guide appropriate treatment and management strategies to mitigate the symptoms and prevent severe complications. The cost of the AKR1D1 Gene Bile Acid Synthesis Defect Type 2 Congenital Genetic Test at DNA Labs UAE is 4400 AED. This investment is crucial for early detection and management of the condition, potentially improving the quality of life for individuals with this genetic disorder.
CYP7B1 Gene Bile acid synthesis defect type 3 congenital Genetic Test Cost
The CYP7B1 Gene Bile Acid Synthesis Defect Type 3 is a rare genetic condition that affects the body's ability to produce bile acids properly. Bile acids are crucial for the digestion and absorption of fats and fat-soluble vitamins. Mutations in the CYP7B1 gene disrupt this process, leading to various health issues, including liver disease, fat malabsorption, and vitamin deficiencies. Early diagnosis and treatment are vital for managing the condition effectively. To diagnose this genetic defect, DNA Labs UAE offers a specialized genetic test targeting the CYP7B1 gene. This test is designed to identify mutations in the gene that are responsible for Bile Acid Synthesis Defect Type 3. The procedure involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed in the laboratory using advanced genetic testing technologies. The cost of the CYP7B1 Gene Bile Acid Synthesis Defect Type 3 congenital genetic test at DNA Labs UAE is 4400 AED. This price includes the cost of the sample collection, genetic analysis, and a comprehensive report detailing the test results. The report is crucial for healthcare providers to develop an appropriate management plan for individuals diagnosed with this condition. Given the specialized nature of this test, it is recommended for individuals with a clinical suspicion of Bile Acid Synthesis Defect Type 3 or those with a family history of the condition. Early and accurate diagnosis can significantly improve the quality of life for affected individuals by enabling targeted treatments and interventions.
AMACR Gene Bile acid synthesis defect type 4 congenital Genetic Test Cost
The "AMACR Gene Bile Acid Synthesis Defect Type 4 Congenital Genetic Test" is a specialized diagnostic assessment conducted to identify mutations in the AMACR gene, which are responsible for a rare disorder known as Bile Acid Synthesis Defect Type 4. This condition is congenital, meaning it is present from birth, and it affects the body's ability to properly synthesize bile acids. These acids are crucial for the digestion and absorption of fats and fat-soluble vitamins. A defect in their synthesis can lead to a variety of health issues, including liver disease, fat malabsorption, and vitamin deficiencies. The test is particularly important for individuals who exhibit symptoms of the disorder or have a family history of bile acid synthesis defects. Early diagnosis through genetic testing can facilitate timely intervention, potentially improving outcomes through dietary management and specific treatments to supplement the deficient bile acids. Performed at DNA Labs UAE, the test involves analyzing the patient's DNA, extracted from a blood sample, to look for mutations in the AMACR gene. The cost of the test is 4400 AED, reflecting the comprehensive analysis and the specialized expertise required to interpret the results. Given the complexity and rarity of the condition, this genetic test is a critical tool for clinicians in diagnosing and managing Bile Acid Synthesis Defect Type 4, enabling personalized treatment plans for affected individuals.
ABCD3 Gene Bile acid synthesis defect type 5 congenital Genetic Test Cost
The ABCD3 Gene Bile Acid Synthesis Defect Type 5 is a rare genetic disorder that disrupts the body's ability to properly produce and process bile acids. These acids are essential for the digestion and absorption of fats and fat-soluble vitamins. Mutations in the ABCD3 gene lead to this condition, which can result in a range of symptoms from mild to severe, including liver dysfunction, fat malabsorption, and vitamin deficiencies. To diagnose this condition, a specific genetic test can be conducted to identify mutations in the ABCD3 gene. This test is crucial for confirming the diagnosis, understanding the severity of the condition, and guiding treatment decisions. It involves analyzing the patient's DNA to look for specific alterations associated with the disorder. In the United Arab Emirates, this genetic test is available at DNA Labs UAE, a leading provider of genetic testing services. The cost of the test is 4400 AED. DNA Labs UAE utilizes state-of-the-art technology to ensure accurate and reliable results, providing essential information for patients and their families dealing with Bile Acid Synthesis Defect Type 5. Early diagnosis and intervention can significantly improve the quality of life for individuals affected by this condition.
