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SLC16A1 Gene Erythrocyte lactate transporter defect Genetic Test Cost
The SLC16A1 gene is crucial for encoding a protein that functions as a lactate transporter in erythrocytes (red blood cells). A defect in this gene can lead to an impaired ability of red blood cells to transport lactate, which may result in various metabolic issues and clinical symptoms. Genetic testing for the SLC16A1 gene erythrocyte lactate transporter defect is an important diagnostic tool for identifying mutations within this gene that could lead to such transporter deficiencies. DNA Labs UAE offers a comprehensive genetic test aimed at detecting mutations in the SLC16A1 gene, helping in the diagnosis of related metabolic conditions. The test involves collecting a DNA sample, typically through a blood draw, and analyzing the genetic material for specific mutations associated with the lactate transporter defect. This precise genetic testing can provide valuable information for the diagnosis, management, and treatment planning for individuals suspected of having this genetic defect. The cost of the SLC16A1 gene erythrocyte lactate transporter defect genetic test at DNA Labs UAE is 4400 AED. This investment covers the expenses associated with the sophisticated laboratory techniques and professional expertise required to accurately identify mutations in the SLC16A1 gene. For patients and healthcare providers, this genetic test is a crucial step towards understanding and managing conditions related to the erythrocyte lactate transporter defect.
GLA Gene Fabry disease Genetic Test Cost
The GLA Gene Fabry Disease Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, designed to detect mutations in the GLA gene, which are responsible for causing Fabry disease. Fabry disease is a rare genetic disorder that impacts various organs and bodily systems, leading to a wide range of symptoms including pain, kidney failure, heart issues, and stroke. The condition is inherited in an X-linked manner, meaning it predominantly affects males, though females can also be carriers and exhibit symptoms. The test involves a detailed analysis of the GLA gene to identify any genetic mutations that may be indicative of Fabry disease. This is crucial for the early diagnosis and management of the condition, allowing for timely intervention and treatment strategies to mitigate the impact of the disease on the individual's health. The cost of the GLA Gene Fabry Disease Genetic Test at DNA Labs UAE is 4400 AED. Given the specialized nature of the test and its potential to significantly influence the management of Fabry disease, it represents a valuable investment in personal health for those at risk or exhibiting symptoms suggestive of this genetic disorder.
F2 Gene Factor II deficiency Genetic Test Cost
The F2 Gene Factor II deficiency genetic test is a specialized diagnostic procedure designed to detect mutations in the F2 gene, which is responsible for the production of prothrombin (factor II) - a protein crucial for proper blood clotting. A deficiency or abnormality in Factor II can lead to either an increased risk of blood clots (thrombosis) or a bleeding disorder, depending on the nature of the mutation. This test is particularly important for individuals with a personal or family history of blood clotting disorders, as it can provide vital information for managing and treating the condition. Conducted at DNA Labs UAE, a leading facility in genetic testing, the test offers a comprehensive analysis of the F2 gene to identify any genetic anomalies that may contribute to clotting disorders. The cost of the F2 Gene Factor II deficiency genetic test is 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify mutations in the gene. By opting for this test, patients can gain valuable insights into their genetic makeup, enabling them and their healthcare providers to make informed decisions about their health management and preventive measures against potential complications associated with Factor II deficiency.
F5 Gene Factor V deficiency Genetic Test Cost
The F5 Gene Factor V Deficiency Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, aimed at identifying mutations in the Factor V gene. Factor V deficiency is a rare genetic disorder that affects the blood's ability to clot properly, leading to an increased risk of bleeding. This condition, also known as Parahemophilia or Owren's disease, can vary in severity and may not manifest symptoms in all individuals. The test specifically looks for genetic variations or mutations in the F5 gene, which codes for the Factor V protein, a crucial component in the blood clotting process. By analyzing a patient's DNA, the test can confirm a diagnosis of Factor V deficiency, help assess the risk of developing the condition, or determine if an individual is a carrier of the gene mutation, which could be passed on to future generations. DNA Labs UAE offers this comprehensive genetic testing service for a cost of 4400 AED. The test is conducted in a state-of-the-art laboratory setting by qualified professionals, ensuring accurate and reliable results. Individuals seeking this test may do so for various reasons, including experiencing symptoms related to blood clotting disorders, having a family history of Factor V deficiency, or planning for future children. In summary, the F5 Gene Factor V Deficiency Genetic Test is a critical tool for diagnosing and managing Factor V deficiency, providing valuable information for affected individuals and their families. Conducted by DNA Labs UAE, this test represents an important step in understanding and addressing genetic factors related to blood clotting disorders.
F13B Gene Factor XIIIB deficiency Genetic Test Cost
The F13B gene factor XIIIB deficiency genetic test is a specialized diagnostic procedure aimed at detecting deficiencies in the Factor XIII B subunit, a crucial protein involved in blood clotting. This test specifically examines the F13B gene for mutations or alterations that could lead to Factor XIII deficiency, a rare genetic disorder that can cause severe bleeding problems. The test is crucial for individuals who have a family history of the disorder or exhibit symptoms related to abnormal bleeding, as early detection can significantly improve management and treatment outcomes. Performed at DNA Labs UAE, a leading facility in genetic diagnostics, the test ensures accuracy and reliability through advanced genomic technologies. The cost of the test is 4400 AED, reflecting the sophisticated nature of the testing process and the specialized expertise required to interpret the results. By identifying specific genetic alterations in the F13B gene, this test plays a pivotal role in guiding clinical decisions, enabling personalized treatment plans, and providing valuable information for family planning to those affected by or at risk of Factor XIII B subunit deficiency.
FANCA Gene Fanconi anemia type A Genetic Test Cost
The FANCA Gene Fanconi Anemia Type A Genetic Test is a specialized diagnostic procedure aimed at identifying mutations in the FANCA gene, which is closely associated with Fanconi anemia type A. This condition is a rare genetic disorder that affects the bone marrow, leading to decreased production of all types of blood cells. People affected by this condition may also have physical abnormalities, an increased risk of certain cancers, and other serious health problems. The test is conducted at DNA Labs UAE, a leading facility in genetic testing and analysis. With a focus on accuracy and confidentiality, DNA Labs UAE provides comprehensive genetic testing services, including the FANCA gene test. This particular test is essential for individuals with a family history of Fanconi anemia or those showing symptoms of the disorder, as early detection can significantly impact the management and treatment of the condition. The cost of the FANCA Gene Fanconi Anemia Type A Genetic Test at DNA Labs UAE is 4400 AED. This price reflects the intricate processes involved in genetic testing, from the extraction and analysis of DNA to the interpretation of results by genetic experts. Although the cost might seem high, the test provides invaluable information that can guide healthcare decisions, inform family planning, and potentially save lives through early intervention.
FANCB Gene Fanconi anemia type B Genetic Test Cost
The "FANCB Gene Fanconi Anemia Type B Genetic Test" is a specialized diagnostic procedure offered at DNA Labs UAE, designed to identify mutations in the FANCB gene, which are responsible for Fanconi anemia type B. Fanconi anemia is a rare genetic disorder that leads to bone marrow failure and increased risk of cancer. The FANCB gene plays a crucial role in the body's ability to repair DNA damage, and mutations in this gene can disrupt this process, leading to the development of the disease. This test is particularly important for individuals with a family history of Fanconi anemia or those presenting symptoms related to the condition, such as physical abnormalities, bone marrow failure, or early onset of cancers. Early detection through the FANCB gene test can facilitate timely intervention and management of the disease, potentially improving the quality of life and survival rates of affected individuals. DNA Labs UAE offers this test at a cost of 4400 AED. The test involves collecting a DNA sample, typically through a blood draw, which is then analyzed in the laboratory for any mutations in the FANCB gene. Results from this test can provide crucial information for families regarding the risk of Fanconi anemia in current or future offspring and can guide decisions regarding genetic counseling and management strategies for the condition.
FANCC Gene Fanconi anemia type C Genetic Test Cost
The "FANCC Gene Fanconi Anemia Type C Genetic Test" is a specialized diagnostic procedure offered at DNA Labs UAE, designed to identify mutations in the FANCC gene, which are associated with Fanconi anemia type C. Fanconi anemia is a rare, inherited blood disorder that leads to bone marrow failure and increased risk of cancer. The FANCC gene plays a crucial role in the DNA repair mechanism, and mutations in this gene can impair cellular functions, leading to the clinical manifestations of the disease. This genetic test is pivotal for individuals with a family history of Fanconi anemia or those exhibiting symptoms related to the disorder, as it can provide definitive confirmation of the condition. Early diagnosis through this test can significantly influence management and treatment strategies, potentially improving patient outcomes. The test is priced at 4400 AED and is conducted in the state-of-the-art facilities of DNA Labs UAE. The laboratory is equipped with the latest technology and staffed by experts in genetic diagnostics, ensuring accurate and reliable results. Individuals undergoing this test can expect a thorough analysis of the FANCC gene for any mutations indicative of Fanconi anemia type C.