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DDC Gene Aromatic L-amino acid decarboxylase deficiency AADC Genetic Test Cost
Aromatic L-amino acid decarboxylase (AADC) deficiency is a rare genetic disorder affecting the way signals are passed between cells in the nervous system. This condition stems from mutations in the DDC gene, which is responsible for the production of the AADC enzyme. This enzyme plays a crucial role in the synthesis of neurotransmitters such as dopamine and serotonin, which are vital for regulating numerous functions in the body, including movement, mood, and behavior. To diagnose this condition, a genetic test can be conducted to identify mutations in the DDC gene. DNA Labs UAE offers a comprehensive genetic test specifically designed to detect these mutations, aiding in the accurate diagnosis of AADC deficiency. The cost of this test is 4400 AED. This genetic testing is crucial for the early diagnosis and management of AADC deficiency. Early diagnosis can lead to interventions that may significantly improve the quality of life for individuals with this condition. The test involves a simple process of collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed in the laboratory for the presence of mutations in the DDC gene. If you suspect you or your child may be showing symptoms of AADC deficiency, or if there's a family history of the condition, it's advisable to discuss the possibility of undergoing genetic testing at DNA Labs UAE with your healthcare provider.
ASNS Gene Asparaginesynthetase deficiency Genetic Test Cost
The ASNS Gene Asparagine Synthetase Deficiency Genetic Test is a specialized diagnostic tool designed to identify mutations in the ASNS gene, which can lead to Asparagine Synthetase Deficiency. This rare and inherited condition disrupts the normal production of the amino acid asparagine, leading to a range of neurological issues, including developmental delay, seizures, and microcephaly. Early and accurate detection through genetic testing is crucial for managing symptoms and improving the quality of life for affected individuals. Performed at DNA Labs UAE, this test is conducted using advanced genetic sequencing techniques to scrutinize the ASNS gene for any abnormalities that might indicate the presence of Asparagine Synthetase Deficiency. The cost of the test is set at 4400 AED, reflecting the intricate technology and expertise required to accurately diagnose this condition. The results from this test can provide essential information for families and healthcare providers, paving the way for targeted interventions and support for those affected by this genetic disorder.
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.
SLC10A2 Gene Bile acid malabsorption primary Genetic Test Cost
The SLC10A2 gene plays a critical role in the body's ability to absorb bile acids, essential components for the digestion and absorption of fats and fat-soluble vitamins in the small intestine. Mutations in the SLC10A2 gene can lead to primary bile acid malabsorption (PBAM), a condition characterized by chronic diarrhea, malnutrition, and a range of gastrointestinal disturbances. To diagnose this condition, a genetic test focusing on the SLC10A2 gene can be conducted. DNA Labs UAE offers this specialized test, providing a comprehensive analysis to detect mutations in the SLC10A2 gene that may lead to PBAM. The test is priced at 4400 AED and is designed to offer insights for individuals experiencing symptoms suggestive of bile acid malabsorption, or for those with a family history of the condition, aiding in the diagnosis and management of PBAM. This genetic test is a crucial step towards personalized treatment plans, dietary adjustments, and improved quality of life 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.