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TALDO1 Gene Transaldolase deficiency Genetic Test Cost
The TALDO1 gene plays a crucial role in the pentose phosphate pathway, a critical metabolic pathway involved in nucleic acid synthesis and the generation of reducing equivalents. Mutations in the TALDO1 gene can lead to transaldolase deficiency, a rare autosomal recessive metabolic disorder that can result in a variety of symptoms including liver dysfunction, developmental delays, and hematological abnormalities. To diagnose this condition, a genetic test for the TALDO1 gene can be conducted. This test is designed to identify mutations in the TALDO1 gene that are responsible for transaldolase deficiency. DNA Labs UAE offers this specific genetic test, providing a crucial diagnostic tool for individuals suspected of having this rare genetic disorder. The cost of the TALDO1 Gene Transaldolase Deficiency Genetic Test at DNA Labs UAE is 4400 AED. This test involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed in the laboratory for the presence of mutations in the TALDO1 gene. The results of this test can help guide treatment decisions and allow for genetic counseling of affected families, offering insights into the condition and its management.
TCN2 Gene Transcobalamin II deficiency Genetic Test Cost
The TCN2 gene plays a crucial role in the body's processing of vitamin B12, an essential nutrient for the development of the nervous system and the production of blood cells. A deficiency in Transcobalamin II, a protein encoded by the TCN2 gene, can lead to a rare but serious condition characterized by megaloblastic anemia, failure to thrive, and neurological disorders due to impaired vitamin B12 transport and cellular uptake. To diagnose this condition, a genetic test focusing on the TCN2 gene can be conducted. This test looks for mutations in the TCN2 gene that are known to cause Transcobalamin II deficiency. Early detection through genetic testing is crucial for managing the condition effectively, as treatment typically involves vitamin B12 supplementation, which can significantly improve outcomes if started early. In the UAE, DNA Labs offers this specific genetic test for Transcobalamin II deficiency. The test is priced at 4400 AED and is conducted in their state-of-the-art facilities. DNA Labs UAE is known for its commitment to providing accurate, reliable, and confidential genetic testing services, ensuring that individuals undergoing the test receive comprehensive support and guidance throughout the testing process.
HADHA Gene Trifunctional protein deficiency Genetic Test Cost
The HADHA gene encodes for a subunit of the mitochondrial trifunctional protein (MTP), an enzyme complex pivotal in the beta-oxidation of long-chain fatty acids. A deficiency in this enzyme, known as Trifunctional Protein Deficiency, can lead to a range of metabolic disorders, presenting various symptoms such as hypoglycemia, cardiomyopathy, liver dysfunction, and muscle weakness. It is a genetic condition that can have severe implications on an individual's health if not diagnosed and managed properly. To diagnose this condition, a genetic test targeting the HADHA gene can be conducted. This test involves analyzing the DNA to identify mutations in the HADHA gene that may lead to Trifunctional Protein Deficiency. It is a crucial step for individuals with a clinical presentation of the disease or for those with a family history, providing them with essential information for management and treatment plans. In the United Arab Emirates, this specific genetic test is available at DNA Labs UAE. The cost of the test is set at 4400 AED. DNA Labs UAE is equipped with advanced genetic testing technologies and staffed by professionals skilled in conducting and interpreting genetic tests, ensuring accurate and reliable results for patients and their families. This test is not only pivotal for diagnosis but also plays a significant role in the genetic counseling process, helping families understand the risk of recurrence in future pregnancies and informing them about potential treatment and management strategies.
FMO3 Gene Trimethylaminuria Genetic Test Cost
The FMO3 gene trimethylaminuria genetic test is a specialized diagnostic procedure aimed at identifying mutations in the FMO3 gene, which are responsible for the condition known as trimethylaminuria, or more commonly referred to as "fish odor syndrome." This genetic disorder impairs the body's ability to break down trimethylamine (TMA), a compound derived from the diet that has a strong fishy odor. As a result, individuals with trimethylaminuria accumulate TMA in their bodies, leading to the emission of a fish-like odor through breath, sweat, and urine, which can significantly impact their social and psychological well-being. 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 FMO3 gene. Identifying these mutations can confirm the diagnosis of trimethylaminuria, enabling healthcare providers to offer appropriate management strategies and dietary advice to help minimize symptoms. In the United Arab Emirates, this genetic test is available at DNA Labs UAE, a leading facility in genetic testing and analysis. The cost of the FMO3 gene trimethylaminuria genetic test at DNA Labs UAE is set at 4400 AED. This investment covers the comprehensive analysis required to detect the presence of mutations in the FMO3 gene, providing crucial information for individuals suspecting they might have this condition or for those seeking confirmation of their diagnosis.
TPI1 Gene Triosephosphate isomerase deficiency Genetic Test Cost
The TPI1 Gene Triosephosphate Isomerase Deficiency Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the TPI1 gene responsible for Triosephosphate Isomerase Deficiency (TPI Deficiency). TPI Deficiency is a rare genetic disorder that affects the body's ability to metabolize carbohydrates properly, leading to a range of symptoms from mild to severe, including hemolytic anemia, neuromuscular abnormalities, and, in some cases, increased susceptibility to infections. This genetic test is crucial for early diagnosis and management of the condition, allowing for tailored treatment plans that can significantly improve the quality of life for affected individuals. The test involves analyzing the patient's DNA to look for specific mutations in the TPI1 gene that are known to cause the disorder. It is a comprehensive test that provides accurate and reliable results, making it an invaluable resource for individuals with a family history of TPI Deficiency or those presenting symptoms suggestive of the disorder. The cost of the TPI1 Gene Triosephosphate Isomerase Deficiency Genetic Test at DNA Labs UAE is 4400 AED. Given the complexity and the specialized nature of this test, the price reflects the advanced technology and expertise required to accurately diagnose this rare genetic condition. Conducting the test at DNA Labs UAE ensures that patients receive the highest standard of care, benefiting from the lab's state-of-the-art facilities and the expertise of its medical professionals.
GALNT3 Gene Tumoral calcinosis hyperphosphatemic familial type 1 Genetic Test Cost
The GALNT3 Gene Test for Tumoral Calcinosis Hyperphosphatemic Familial Type 1 is a specialized genetic test available at DNA Labs UAE, designed to diagnose this rare genetic disorder. Tumoral calcinosis hyperphosphatemic familial type 1 is characterized by the abnormal deposition of calcium phosphate in the skin and other tissues, leading to painful lumps. This condition is caused by mutations in the GALNT3 gene, which plays a crucial role in regulating phosphate levels in the body. The test involves analyzing the patient's DNA to identify mutations in the GALNT3 gene, providing crucial information for diagnosis, treatment planning, and genetic counseling. By pinpointing the exact genetic cause of the condition, healthcare providers can offer more targeted and effective interventions. At DNA Labs UAE, the cost of the GALNT3 Gene Test for Tumoral Calcinosis Hyperphosphatemic Familial Type 1 is set at 4400 AED. This cost reflects the comprehensive nature of the test, encompassing the sophisticated techniques and expertise required to accurately identify mutations in the GALNT3 gene. Patients and families opting for this test can expect reliable results, contributing to a better understanding of the condition and guiding the path forward for management and care.
FAH Gene Tyrosinemia type 1 Genetic Test Cost
The FAH Gene Tyrosinemia Type 1 Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to detect mutations in the FAH gene, which are responsible for Tyrosinemia type 1. Tyrosinemia type 1 is a rare genetic disorder that affects the body's ability to metabolize the amino acid tyrosine, leading to liver disease, kidney problems, and neurological issues if left untreated. Early detection through this genetic test can be crucial for initiating timely treatment strategies, such as dietary management and medication, to prevent severe complications. DNA Labs UAE offers this test at a cost of 4400 AED. The process involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed in the lab for the presence of specific mutations in the FAH gene. Results from this test can provide valuable information for affected individuals and their families regarding the management of Tyrosinemia type 1, including considerations for genetic counseling and potential treatment plans.
GSTZ1 Gene Tyrosinemia type 1B Genetic Test Cost
The "GSTZ1 Gene Tyrosinemia Type 1B Genetic Test" is a specialized diagnostic procedure offered by DNA Labs UAE, aimed at detecting mutations in the GSTZ1 gene, which are linked to Tyrosinemia type 1B, a rare genetic disorder. This condition affects the body's ability to properly break down the amino acid tyrosine, leading to various health issues, including liver and kidney problems. The test is crucial for early detection and management of the disorder, enabling healthcare providers to tailor appropriate treatment plans for affected individuals. The cost of the test is set at 4400 AED, reflecting the comprehensive analysis and expertise required to accurately identify the genetic variations associated with Tyrosinemia type 1B.
